MCID: AND005
MIFTS: 16

Androgen Insensitivity Syndrome, Mild

Categories: Rare diseases, Genetic diseases

Aliases & Classifications for Androgen Insensitivity Syndrome, Mild

MalaCards integrated aliases for Androgen Insensitivity Syndrome, Mild:

Name: Androgen Insensitivity Syndrome, Mild 50 29
Mild Androgen Insensitivity Syndrome 50 24
Mais 50 24
Undervirilized Male Syndrome 50

Classifications:



Summaries for Androgen Insensitivity Syndrome, Mild

MalaCards based summary : Androgen Insensitivity Syndrome, Mild, also known as mild androgen insensitivity syndrome, is related to may-hegglin anomaly and may-thurner syndrome.

Related Diseases for Androgen Insensitivity Syndrome, Mild

Diseases related to Androgen Insensitivity Syndrome, Mild via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 4708, show less)
id Related Disease Score Top Affiliating Genes
1 may-hegglin anomaly 12.2
2 may-thurner syndrome 12.1
3 mycobacterium avium complex disease 11.2
4 myh9 related thrombocytopenia 11.2
5 prostate cancer 10.7
6 breast cancer 10.7
7 essential tremor 10.6
8 lupus erythematosus 10.6
9 schizophrenia 10.6
10 encephalitis 10.6
11 crohn's disease 10.6
12 dermatomyositis 10.6
13 vaginitis 10.6
14 herpes zoster 10.6
15 syringomyelia 10.6
16 multiple myeloma 10.6
17 pancreatitis 10.6
18 hydrocephalus 10.6
19 hepatitis 10.6
20 dermatitis 10.6
21 myasthenia gravis 10.6
22 cushing's syndrome 10.6
23 meningitis 10.6
24 pertussis 10.6
25 dyspepsia 10.6
26 lyme disease 10.6
27 diarrhea 10.6
28 twin-to-twin transfusion syndrome 10.6
29 hypogonadotropic hypogonadism 10.6
30 thoracic outlet syndrome 10.6
31 chronic pain 10.6
32 leukemia 10.6
33 fatty liver disease 10.6
34 celiac disease 10.5
35 osteogenesis imperfecta 10.5
36 agnosia 10.5
37 asthma 10.5
38 back pain 10.5
39 fainting 10.5
40 neuroblastoma 10.5
41 panic disorder 10.5
42 tardive dyskinesia 10.5
43 autism spectrum disorder 10.5
44 palindromic rheumatism 10.5
45 dementia 10.5
46 peritonitis 10.5
47 rheumatoid arthritis 10.5
48 traumatic brain injury 10.5
49 hereditary spastic paraplegia 10.5
50 apraxia 10.5
51 stomach cancer 10.5
52 meniere's disease 10.5
53 lung cancer 10.5
54 melanoma 10.5
55 alzheimer disease 10.5
56 arachnoiditis 10.5
57 muscular dystrophy 10.5
58 chronic lymphocytic leukemia 10.5
59 graves' disease 10.5
60 lymphoma 10.5
61 menkes disease 10.5
62 tonsillitis 10.5
63 uterine fibroid 10.5
64 myotonic dystrophy 10.5
65 narcolepsy 10.5
66 kawasaki disease 10.5
67 thalassemia 10.5
68 glioblastoma 10.5
69 down syndrome 10.5
70 hemochromatosis 10.5
71 gastroschisis 10.5
72 cholera 10.5
73 complex regional pain syndrome 10.5
74 mercury poisoning 10.5
75 epilepsy 10.5
76 hepatitis c 10.5
77 microcephaly 10.5
78 porphyria 10.5
79 congenital diaphragmatic hernia 10.5
80 ovarian cyst 10.5
81 erythromelalgia 10.5
82 esophageal cancer 10.5
83 cataract 10.5
84 cystic fibrosis 10.5
85 pancreatic cancer 10.5
86 influenza 10.5
87 squamous cell carcinoma 10.5
88 leigh syndrome 10.5
89 buschke-ollendorff syndrome 10.5
90 gilles de la tourette syndrome 10.5
91 microphthalmia 10.5
92 myotonia congenita 10.5
93 cor triatriatum 10.5
94 hepatitis b 10.5
95 trigeminal neuralgia 10.5
96 postpartum depression 10.5
97 bipolar disorder 10.5
98 sleep apnea 10.5
99 myocardial infarction 10.5
100 myelodysplastic syndrome 10.5
101 acromegaly 10.5
102 hiv-1 10.5
103 cerebral palsy 10.5
104 dystonia 10.5
105 glomerulonephritis 10.5
106 restless legs syndrome 10.5
107 gastritis 10.5
108 herpes simplex 10.5
109 tremor 10.5
110 charcot-marie-tooth disease 10.5
111 neuroleptic malignant syndrome 10.5
112 rubella 10.5
113 polymyositis 10.5
114 obesity 10.5
115 otitis media 10.5
116 abdominal aortic aneurysm 10.5
117 colorectal cancer 10.5
118 headache 10.5
119 interstitial lung disease 10.5
120 chronic fatigue syndrome 10.5
121 krabbe disease 10.5
122 temporal arteritis 10.5
123 waldenstrom macroglobulinemia 10.5
124 chikungunya 10.5
125 klippel-feil syndrome 10.5
126 nephrocalcinosis 10.5
127 cystic lymphangioma 10.5
128 cellulitis 10.5
129 reactive arthritis 10.5
130 pseudocholinesterase deficiency 10.5
131 systemic onset juvenile idiopathic arthritis 10.5
132 angiomatosis 10.5
133 diffuse large b-cell lymphoma 10.4
134 huntington disease 10.4
135 attention deficit-hyperactivity disorder 10.4
136 diabetic neuropathy 10.4
137 tetanus 10.4
138 ehlers-danlos syndrome 10.4
139 ulcerative colitis 10.4
140 syncope 10.4
141 polycystic ovary syndrome 10.4
142 cardiomyopathy 10.4
143 friedreich ataxia 10.4
144 lactose intolerance 10.4
145 diphtheria 10.4
146 craniopharyngioma 10.4
147 prion disease 10.4
148 neural tube defects 10.4
149 brain injury 10.4
150 b-cell lymphomas 10.4
151 esophagitis 10.4
152 van der woude syndrome 10.4
153 hypoplastic left heart syndrome 10.4
154 chagas disease 10.4
155 hepatitis a 10.4
156 tuberous sclerosis 10.4
157 acute disseminated encephalomyelitis 10.4
158 endocarditis 10.4
159 personality disorder 10.4
160 hemophilia 10.4
161 coronary artery disease 10.4
162 aplastic anemia 10.4
163 mycosis fungoides 10.4
164 spinal muscular atrophy 10.4
165 hepatic encephalopathy 10.4
166 polyneuropathy 10.4
167 hypogonadism 10.4
168 teratoma 10.4
169 irritable bowel syndrome 10.4
170 malaria 10.4
171 osteoporosis 10.4
172 atrial fibrillation 10.4
173 budd-chiari syndrome 10.4
174 aniridia 10.4
175 trichotillomania 10.4
176 adrenoleukodystrophy 10.4
177 macroglossia 10.4
178 west syndrome 10.4
179 osteopetrosis 10.4
180 latex allergy 10.4
181 hepatic veno-occlusive disease 10.4
182 cysticercosis 10.4
183 guillain-barre syndrome 10.4
184 transient cerebral ischemia 10.4
185 ankylosis 10.4
186 intestinal pseudo-obstruction 10.4
187 peptic ulcer disease 10.4
188 eccrine porocarcinoma 10.4
189 septic arthritis 10.4
190 gigantism 10.4
191 pseudobulbar affect 10.4
192 thyrotoxic periodic paralysis 10.4
193 wells syndrome 10.4
194 hypersomnia 10.4
195 osteoarthritis 10.4
196 riboflavin deficiency 10.4
197 arthritis 10.4
198 sebastian syndrome 10.4
199 pemphigus 10.4
200 peripheral artery disease 10.4
201 nasopharyngitis 10.4
202 hereditary spherocytosis 10.4
203 interstitial cystitis 10.4
204 candidiasis 10.4
205 normal pressure hydrocephalus 10.4
206 anxiety disorder 10.4
207 long qt syndrome 10.4
208 aneurysm 10.4
209 systemic lupus erythematosus 10.4
210 psoriasis 10.4
211 heart disease 10.4
212 endometriosis 10.4
213 machado-joseph disease 10.4
214 fechtner syndrome 10.4
215 cervical dystonia 10.4
216 osteomyelitis 10.4
217 common cold 10.4
218 bell's palsy 10.4
219 food allergy 10.4
220 burning mouth syndrome 10.4
221 toxoplasmosis 10.4
222 adenomyosis 10.4
223 arachnoid cysts 10.4
224 leukoplakia 10.4
225 head injury 10.4
226 whiplash 10.4
227 retinitis 10.4
228 insulin-like growth factor i 10.4
229 hailey-hailey disease 10.4
230 moyamoya disease 10.4
231 stiff-person syndrome 10.4
232 adiposis dolorosa 10.4
233 breast reconstruction 10.4
234 chronic granulomatous disease 10.4
235 hellp syndrome 10.4
236 brain cancer 10.4
237 nemaline myopathy 10.4
238 liposarcoma 10.4
239 superior mesenteric artery syndrome 10.4
240 porokeratosis 10.4
241 aphthous stomatitis 10.4
242 chronic thromboembolic pulmonary hypertension 10.4
243 fibromuscular dysplasia 10.4
244 mollaret meningitis 10.4
245 pancreatic neuroendocrine tumor 10.4
246 soft tissue sarcoma 10.4
247 hodgkin lymphoma 10.4
248 motor neuron disease 10.4
249 constipation 10.4
250 glioma 10.4
251 encephalopathy 10.4
252 hepatocellular carcinoma 10.4
253 biotinidase deficiency 10.4
254 cleidocranial dysplasia 10.4
255 burkitt lymphoma 10.4
256 factor x deficiency 10.4
257 pityriasis rubra pilaris 10.4
258 ewing sarcoma 10.4
259 barth syndrome 10.4
260 coats disease 10.4
261 keratoconus 10.4
262 brugada syndrome 10.4
263 depersonalization disorder 10.4
264 brucellosis 10.4
265 glossopharyngeal neuralgia 10.4
266 granular cell tumor 10.4
267 protein c deficiency 10.4
268 vaginal discharge 10.4
269 prosopagnosia 10.4
270 epithelioid sarcoma 10.4
271 scabies 10.4
272 bullous pemphigoid 10.4
273 croup 10.4
274 median arcuate ligament syndrome 10.4
275 mitochondrial disorders 10.4
276 amniotic band syndrome 10.4
277 cor triatriatum sinister 10.4
278 malakoplakia 10.4
279 meralgia paresthetica 10.4
280 pemphigoid gestationis 10.4
281 tracheoesophageal fistula 10.4
282 myotonia 10.4
283 inclusion body myositis 10.4
284 legionnaires' disease 10.4
285 optic neuritis 10.4
286 hidradenitis suppurativa 10.4
287 thymoma 10.4
288 hypoglycemia 10.4
289 polycystic kidney disease 10.4
290 conjunctivitis 10.4
291 diverticulitis 10.4
292 hyperthyroidism 10.4
293 dermatofibrosarcoma protuberans 10.4
294 sinusitis 10.4
295 ectopic pregnancy 10.4
296 rift valley fever 10.4
297 adult-onset still's disease 10.4
298 gastric adenocarcinoma 10.4
299 merkel cell carcinoma 10.4
300 myoclonus 10.4
301 tuberculosis 10.4
302 thrombosis 10.4
303 kidney disease 10.3
304 creutzfeldt-jakob disease 10.3
305 paroxysmal nocturnal hemoglobinuria 10.3
306 lemierre's syndrome 10.3
307 schistosomiasis 10.3
308 turner syndrome 10.3
309 syphilis 10.3
310 avian influenza 10.3
311 retinal detachment 10.3
312 myocarditis 10.3
313 hemicrania continua 10.3
314 limbic encephalitis 10.3
315 atopic dermatitis 10.3
316 cervicitis 10.3
317 osteonecrosis 10.3
318 gastrointestinal stromal tumor 10.3
319 beckwith-wiedemann syndrome 10.3
320 marfan syndrome 10.3
321 epstein syndrome 10.3
322 becker muscular dystrophy 10.3
323 yellow nail syndrome 10.3
324 adult t-cell leukemia 10.3
325 holoprosencephaly 10.3
326 lissencephaly 10.3
327 lennox-gastaut syndrome 10.3
328 zollinger-ellison syndrome 10.3
329 congenital adrenal hyperplasia 10.3
330 leukodystrophy 10.3
331 echinococcosis 10.3
332 kidney cancer 10.3
333 hepatoblastoma 10.3
334 chickenpox 10.3
335 brittle diabetes 10.3
336 cluster headache 10.3
337 pulmonary arteriovenous malformation 10.3
338 retroperitoneal fibrosis 10.3
339 cytomegalovirus infection 10.3
340 patent foramen ovale 10.3
341 cystitis 10.3
342 myositis 10.3
343 spasticity 10.3
344 colitis 10.3
345 male infertility 10.3
346 poliomyelitis 10.3
347 oral cancer 10.3
348 leprosy 10.3
349 pulmonary hypertension 10.3
350 hypothyroidism 10.3
351 atherosclerosis 10.3
352 melioidosis 10.3
353 pulmonary alveolar microlithiasis 10.3
354 kleefstra syndrome 10.3
355 autoimmune lymphoproliferative syndrome 10.3
356 exfoliation syndrome 10.3
357 acth-independent macronodular adrenal hyperplasia 10.3
358 pulmonary atresia with ventricular septal defect 10.3
359 hypomelanosis of ito 10.3
360 peyronie's disease 10.3
361 hemophagocytic lymphohistiocytosis 10.3
362 collagenous colitis 10.3
363 robinow syndrome 10.3
364 pigment dispersion syndrome 10.3
365 congenital myopathy 10.3
366 sleeping sickness 10.3
367 rickets 10.3
368 cat-scratch disease 10.3
369 bulimia nervosa 10.3
370 megaloblastic anemia 10.3
371 coccidioidomycosis 10.3
372 rheumatic fever 10.3
373 impotence 10.3
374 bursitis 10.3
375 inverted papilloma 10.3
376 mixed connective tissue disease 10.3
377 agoraphobia 10.3
378 autoimmune hemolytic anemia 10.3
379 zellweger syndrome 10.3
380 trichinosis 10.3
381 refractive error 10.3
382 congenital cytomegalovirus 10.3
383 frontal fibrosing alopecia 10.3
384 hansen's disease 10.3
385 hemiplegic migraine 10.3
386 notalgia paresthetica 10.3
387 pulmonary sequestration 10.3
388 synovial chondromatosis 10.3
389 talipes equinovarus 10.3
390 hereditary neuropathies 10.3
391 megalencephaly 10.3
392 mini stroke 10.3
393 paresthesia 10.3
394 aspergillosis 10.3
395 hemophilia a 10.3
396 relapsing-remitting multiple sclerosis 10.3
397 artery disease 10.3
398 prader-willi syndrome 10.3
399 psoriatic arthritis 10.3
400 gastroesophageal reflux 10.3
401 androgen insensitivity 10.3
402 fragile x syndrome 10.3
403 alcoholic hepatitis 10.3
404 bronchiolitis obliterans 10.3
405 hemolytic-uremic syndrome 10.3
406 basal cell carcinoma 10.3
407 epidermolysis bullosa 10.3
408 dyslexia 10.3
409 malignant hyperthermia 10.3
410 dysphagia 10.3
411 pneumonia 10.3
412 hepatitis c virus 10.3
413 wiskott-aldrich syndrome 10.3
414 pulmonary fibrosis 10.3
415 sacrococcygeal teratoma 10.3
416 familial adenomatous polyposis 10.3
417 distal arthrogryposis 10.3
418 osteomalacia 10.3
419 urinary bladder cancer 10.3
420 pneumothorax 10.3
421 hypokalemia 10.3
422 rosacea 10.3
423 pulmonary embolism 10.3
424 alopecia areata 10.3
425 lichen sclerosus 10.3
426 oral lichen planus 10.3
427 hydranencephaly 10.3
428 hyperprolactinemia 10.3
429 phenylketonuria 10.3
430 rett syndrome 10.3
431 deficiency anemia 10.3
432 sertoli cell-only syndrome 10.3
433 silicosis 10.3
434 pelvic inflammatory disease 10.3
435 pre-eclampsia 10.3
436 short bowel syndrome 10.3
437 portal hypertension 10.3
438 q fever 10.3
439 cardiac tamponade 10.3
440 iron deficiency anemia 10.3
441 essential thrombocythemia 10.3
442 meige syndrome 10.3
443 progressive multifocal leukoencephalopathy 10.3
444 clear cell renal cell carcinoma 10.3
445 goblet cell carcinoid 10.3
446 adenoma 10.3
447 wolf-hirschhorn syndrome 10.3
448 rothmund-thomson syndrome 10.3
449 alport syndrome 10.3
450 reflex sympathetic dystrophy 10.3
451 gingival recession 10.3
452 post-transplant lymphoproliferative disease 10.3
453 retinitis pigmentosa 10.3
454 spinal cord injury 10.3
455 rocky mountain spotted fever 10.3
456 cutaneous t cell lymphoma 10.3
457 dowling-degos disease 10.3
458 mumps 10.3
459 legionellosis 10.3
460 intracranial aneurysm 10.3
461 meconium aspiration syndrome 10.3
462 gout 10.3
463 toxic shock syndrome 10.3
464 cheilitis 10.3
465 pericarditis 10.3
466 post-traumatic stress disorder 10.3
467 protein s deficiency 10.3
468 testicular cancer 10.3
469 oligodendroglioma 10.3
470 causalgia 10.3
471 bacterial vaginosis 10.3
472 necrobiosis lipoidica 10.3
473 kallmann syndrome 10.3
474 lynch syndrome 10.3
475 nail disease 10.3
476 folliculitis 10.3
477 epidermolysis bullosa simplex 10.3
478 pilocytic astrocytoma 10.3
479 impetigo 10.3
480 birth defects 10.3
481 sickle cell disease 10.3
482 cold urticaria 10.3
483 corticobasal degeneration 10.3
484 cyclic vomiting syndrome 10.3
485 diffuse cutaneous systemic sclerosis 10.3
486 orofacial granulomatosis 10.3
487 chronic progressive external ophthalmoplegia 10.3
488 central pain syndrome 10.3
489 psychogenic movement 10.3
490 thyroid cancer 10.2
491 neuromyelitis optica 10.2
492 pycnodysostosis 10.2
493 leiomyomatosis and renal cell cancer 10.2
494 complement factor i deficiency 10.2
495 oculodentodigital dysplasia 10.2
496 spinocerebellar ataxia 1 10.2
497 sickle cell anemia 10.2
498 keratitis 10.2
499 osteoporosis-pseudoglioma syndrome 10.2
500 ulnar-mammary syndrome 10.2
501 holt-oram syndrome 10.2
502 oculopharyngeal muscular dystrophy 10.2
503 gitelman syndrome 10.2
504 canavan disease 10.2
505 potocki-lupski syndrome 10.2
506 smith-magenis syndrome 10.2
507 alexander disease 10.2
508 marden-walker syndrome 10.2
509 spinocerebellar ataxia 6 10.2
510 pseudopseudohypoparathyroidism 10.2
511 phelan-mcdermid syndrome 10.2
512 lowe syndrome 10.2
513 rippling muscle disease 10.2
514 scurvy 10.2
515 joint disorders 10.2
516 megakaryocytic leukemia 10.2
517 neonatal stroke 10.2
518 severe congenital neutropenia 10.2
519 antley-bixler syndrome 10.2
520 inflammatory myofibroblastic tumor 10.2
521 myelomeningocele 10.2
522 dysplastic nevus syndrome 10.2
523 xerophthalmia 10.2
524 pleurisy 10.2
525 giardiasis 10.2
526 hand, foot and mouth disease 10.2
527 wernicke-korsakoff syndrome 10.2
528 hypoparathyroidism 10.2
529 osteopoikilosis 10.2
530 acoustic neuroma 10.2
531 nephronophthisis 10.2
532 tolosa-hunt syndrome 10.2
533 keratoconjunctivitis sicca 10.2
534 hypophosphatasia 10.2
535 autosomal dominant cerebellar ataxia 10.2
536 neuronal ceroid lipofuscinosis 10.2
537 hereditary angioedema 10.2
538 lymphangioma 10.2
539 richter's syndrome 10.2
540 cryptosporidiosis 10.2
541 coccidiosis 10.2
542 leptospirosis 10.2
543 kernicterus 10.2
544 cockayne syndrome 10.2
545 substance abuse 10.2
546 angiomyolipoma 10.2
547 calciphylaxis 10.2
548 ganglioglioma 10.2
549 blepharospasm 10.2
550 gliomatosis cerebri 10.2
551 pyoderma gangrenosum 10.2
552 epiglottitis 10.2
553 polyarteritis nodosa 10.2
554 ataxia with vitamin e deficiency 10.2
555 acquired angioedema 10.2
556 acute respiratory distress syndrome 10.2
557 auditory neuropathy 10.2
558 carcinoid syndrome 10.2
559 cerebrospinal fluid leak 10.2
560 complete androgen insensitivity syndrome 10.2
561 desmoid tumor 10.2
562 hhv-6 encephalitis 10.2
563 idiopathic neutropenia 10.2
564 infantile apnea 10.2
565 meningococcal infection 10.2
566 nodular regenerative hyperplasia 10.2
567 pulmonary vein stenosis 10.2
568 reversible cerebral vasoconstriction syndrome 10.2
569 scleromyxedema 10.2
570 hyperammonemia 10.2
571 cerebral aneurysms 10.2
572 neurosarcoidosis 10.2
573 postural hypotension 10.2
574 shaken baby syndrome 10.2
575 albinism, oculocutaneous, type ii 10.2
576 ocular motor apraxia 10.2
577 hemifacial atrophy, progressive 10.2
578 niemann-pick disease 10.2
579 vitreoretinochoroidopathy dominant 10.2
580 hematopoietic stem cell transplantation 10.2
581 neutropenia 10.2
582 azoospermia 10.2
583 cryptorchidism 10.2
584 acute pancreatitis 10.2
585 vasculitis 10.2
586 autonomic dysfunction 10.2
587 melanocytic nevus syndrome, congenital, somatic 10.2
588 parkinson disease, late-onset 10.2
589 alternating hemiplegia of childhood 10.2
590 schizencephaly 10.2
591 centronuclear myopathy, autosomal, modifier of 10.2
592 cardiomyopathy, familial hypertrophic 10.2
593 dandy-walker syndrome 10.2
594 peroxisome biogenesis disorder 1b 10.2
595 melkersson-rosenthal syndrome 10.2
596 fabry disease 10.2
597 empty sella syndrome 10.2
598 burns 10.2
599 dilated cardiomyopathy 10.2
600 liver cirrhosis 10.2
601 neuritis 10.2
602 lateral sclerosis 10.2
603 newcastle disease 10.2
604 lichen planus 10.2
605 focal segmental glomerulosclerosis 10.2
606 intrahepatic cholangiocarcinoma 10.2
607 bartter syndrome, type 3 10.2
608 hypokalemic periodic paralysis, type 1 10.2
609 dementia, lewy body 10.2
610 papillorenal syndrome 10.2
611 dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema 10.2
612 chromosome 3q29 deletion syndrome 10.2
613 kleine-levin hibernation syndrome 10.2
614 tethered spinal cord syndrome 10.2
615 shigellosis 10.2
616 congenital myasthenic syndrome 10.2
617 episodic ataxia 10.2
618 proximal spinal muscular atrophy 10.2
619 sudden infant death syndrome 10.2
620 medulloblastoma 10.2
621 adenoiditis 10.2
622 aspiration pneumonia 10.2
623 scoliosis 10.2
624 respiratory failure 10.2
625 sapho syndrome 10.2
626 dracunculiasis 10.2
627 bruxism 10.2
628 antiphospholipid syndrome 10.2
629 laryngitis 10.2
630 duodenitis 10.2
631 learning disability 10.2
632 amyloidosis 10.2
633 pheochromocytoma 10.2
634 multiple system atrophy 10.2
635 anorexia nervosa 10.2
636 hypertriglyceridemia 10.2
637 arteriovenous fistula 10.2
638 autoimmune hepatitis 10.2
639 bone fracture 10.2
640 temporal lobe epilepsy 10.2
641 vitamin b12 deficiency 10.2
642 infective endocarditis 10.2
643 cardiac arrest 10.2
644 arteriovenous malformation 10.2
645 pulmonary edema 10.2
646 myopia 10.2
647 addison's disease 10.2
648 ichthyosis 10.2
649 viral hepatitis 10.2
650 motion sickness 10.2
651 myelitis 10.2
652 mood disorder 10.2
653 appendicitis 10.2
654 achalasia 10.2
655 autoimmune pancreatitis 10.2
656 chronic graft versus host disease 10.2
657 germ cells tumors 10.2
658 nodding syndrome 10.2
659 nodular lymphocyte predominant hodgkin lymphoma 10.2
660 epidermal nevus, somatic 10.2
661 popliteal pterygium syndrome 1 10.2
662 multiple sclerosis, disease progression, modifier of 10.2
663 aicardi-goutieres syndrome 1, dominant and recessive 10.2
664 spondyloarthropathy 1 10.2
665 dentin dysplasia, type i, with microdontia and misshapen teeth 10.2
666 coloboma of optic nerve 10.2
667 aromatase deficiency 10.2
668 pneumothorax, primary spontaneous 10.2
669 adie pupil 10.2
670 pain disorder 10.2
671 yaws 10.2
672 hiatus hernia 10.2
673 sjogren's syndrome 10.2
674 whipple disease 10.2
675 autosomal dominant optic atrophy plus syndrome 10.2
676 beryllium disease 10.2
677 chiari malformation 10.2
678 cobb syndrome 10.2
679 febrile infection-related epilepsy syndrome 10.2
680 grover's disease 10.2
681 leydig cell hypoplasia 10.2
682 mal de debarquement 10.2
683 spasmodic dysphonia 10.2
684 swallowing disorders 10.2
685 allergic rhinitis 10.2
686 membranous nephropathy 10.2
687 h. pylori infection 10.2
688 digeorge syndrome 10.2
689 anaplastic large cell lymphoma 10.2
690 common variable immunodeficiency 10.2
691 craniosynostosis 10.2
692 severe combined immunodeficiency 10.2
693 spinal stenosis 10.2
694 paraganglioma 10.2
695 esophageal atresia 10.2
696 borderline personality disorder 10.2
697 spotted fever 10.2
698 transient global amnesia 10.2
699 eclampsia 10.2
700 frozen shoulder 10.2
701 oligospermia 10.2
702 angioedema 10.2
703 myeloproliferative neoplasm 10.2
704 pharyngitis 10.2
705 wernicke encephalopathy 10.2
706 psychotic disorder 10.2
707 struma ovarii 10.2
708 carotid artery disease 10.2
709 arthropathy 10.2
710 eating disorder 10.2
711 smallpox 10.2
712 actinic keratosis 10.2
713 cervical intraepithelial neoplasia 10.2
714 charles bonnet syndrome 10.2
715 nephrogenic systemic fibrosis 10.2
716 plasma cell leukemia 10.2
717 primary central nervous system lymphoma 10.2
718 weber syndrome 10.2
719 dysautonomia 10.2
720 paraneoplastic syndromes 10.2
721 west nile virus 10.1
722 shwachman-diamond syndrome 10.1
723 mucopolysaccharidosis vii 10.1
724 denys-drash syndrome 10.1
725 angelman syndrome 10.1
726 nonarteritic anterior ischemic optic neuropathy 10.1
727 pelizaeus-merzbacher disease 10.1
728 lesch-nyhan syndrome 10.1
729 peripheral vascular disease 10.1
730 end stage renal failure 10.1
731 nephrolithiasis 10.1
732 primary ciliary dyskinesia 10.1
733 thrombotic thrombocytopenic purpura 10.1
734 methemoglobinemia 10.1
735 tooth disease 10.1
736 cicatricial pemphigoid 10.1
737 hepatorenal syndrome 10.1
738 gastroparesis 10.1
739 sympathetic ophthalmia 10.1
740 crimean-congo hemorrhagic fever 10.1
741 dysentery 10.1
742 leiomyoma 10.1
743 opisthorchiasis 10.1
744 glossitis 10.1
745 bone cancer 10.1
746 telogen effluvium 10.1
747 hyperostosis 10.1
748 tularemia 10.1
749 gastroenteritis 10.1
750 angiodysplasia 10.1
751 cryoglobulinemia 10.1
752 pseudomyxoma peritonei 10.1
753 choriocarcinoma 10.1
754 endometrial stromal sarcoma 10.1
755 prostate disease 10.1
756 leiomyomatosis 10.1
757 lipodystrophy 10.1
758 dermatitis herpetiformis 10.1
759 dermatophytosis 10.1
760 diabetes insipidus 10.1
761 plantar fasciitis 10.1
762 hydrocele 10.1
763 cocaine dependence 10.1
764 eosinophilia-myalgia syndrome 10.1
765 limb-girdle muscular dystrophy 10.1
766 autoimmune encephalitis 10.1
767 central serous chorioretinopathy 10.1
768 dwarfism 10.1
769 intravascular papillary endothelial hyperplasia 10.1
770 linear porokeratosis 10.1
771 lymphocytic hypophysitis 10.1
772 monogenic diabetes 10.1
773 nonalcoholic steatohepatitis 10.1
774 transverse myelitis 10.1
775 ulcerative proctitis 10.1
776 hypotonia 10.1
777 serotonin syndrome 10.1
778 peroxisome biogenesis disorder 6b 10.1
779 leukoencephalopathy with vanishing white matter 10.1
780 neurocutaneous melanosis, somatic 10.1
781 pyruvate kinase deficiency 10.1
782 peroxisome biogenesis disorder 11b 10.1
783 wolcott-rallison syndrome 10.1
784 von hippel-lindau syndrome 10.1
785 ovarian cancer, somatic 10.1
786 nephrolithiasis, calcium oxalate 10.1
787 alpha-methylacyl-coa racemase deficiency 10.1
788 sotos syndrome 1 10.1
789 peroxisome biogenesis disorder 4b 10.1
790 aromatic l-amino acid decarboxylase deficiency 10.1
791 argininosuccinic aciduria 10.1
792 dystonia-11, myoclonic 10.1
793 osteofibrous dysplasia 10.1
794 sengers syndrome 10.1
795 farber lipogranulomatosis 10.1
796 peroxisome biogenesis disorder 5b 10.1
797 joubert syndrome 1 10.1
798 myopathy, tubular aggregate, 1 10.1
799 pituitary adenoma, acth-secreting 10.1
800 immunodeficiency 17, cd3 gamma deficient 10.1
801 peroxisome biogenesis disorder 2b 10.1
802 darier disease 10.1
803 neurofibromatosis, type 1 10.1
804 peroxisome biogenesis disorder 3b 10.1
805 gerstmann-straussler disease 10.1
806 peroxisome biogenesis disorder 7b 10.1
807 linear skin defects with multiple congenital anomalies 1 10.1
808 aarskog-scott syndrome 10.1
809 spinal and bulbar muscular atrophy of kennedy 10.1
810 mohr-tranebjaerg syndrome 10.1
811 cerebral creatine deficiency syndrome 1 10.1
812 46xx sex reversal 1 10.1
813 duchenne muscular dystrophy 10.1
814 behcet syndrome 10.1
815 panencephalitis, subacute sclerosing 10.1
816 alpha 1-antitrypsin deficiency 10.1
817 adams-oliver syndrome 10.1
818 von willebrand's disease 10.1
819 tooth ankylosis 10.1
820 de quervain disease 10.1
821 gaucher's disease 10.1
822 unverricht-lundborg syndrome 10.1
823 mesangial proliferative glomerulonephritis 10.1
824 salivary gland adenoid cystic carcinoma 10.1
825 anthrax disease 10.1
826 hereditary paraganglioma-pheochromocytoma syndromes 10.1
827 carnitine palmitoyltransferase i deficiency , muscle 10.1
828 diencephalic syndrome 10.1
829 harding ataxia 10.1
830 myoclonic astatic epilepsy 10.1
831 opsoclonus-myoclonus syndrome 10.1
832 paroxysmal hemicrania 10.1
833 perniosis 10.1
834 pityriasis lichenoides 10.1
835 postural orthostatic tachycardia syndrome 10.1
836 prinzmetal's variant angina 10.1
837 split spinal cord malformation 10.1
838 tethered cord syndrome 10.1
839 x-linked dystonia-parkinsonism/lubag 10.1
840 familial spastic paralysis 10.1
841 myopathy - thyrotoxic 10.1
842 renal tubular dysgenesis 10.1
843 buruli ulcer 10.1
844 crigler-najjar syndrome, type i 10.1
845 thyroid hormone resistance 10.1
846 cerebellar ataxia 10.1
847 achondroplasia 10.1
848 cherubism 10.1
849 wolfram syndrome 10.1
850 williams-beuren syndrome 10.1
851 charge syndrome 10.1
852 pendred syndrome 10.1
853 wolff-parkinson-white syndrome 10.1
854 werner syndrome 10.1
855 omenn syndrome 10.1
856 charcot-marie-tooth disease, type 1a 10.1
857 peho syndrome 10.1
858 intervertebral disc disease 10.1
859 cat eye syndrome 10.1
860 iron-refractory iron deficiency anemia 10.1
861 retinoschisis 10.1
862 ornithine transcarbamylase deficiency 10.1
863 borjeson-forssman-lehmann syndrome 10.1
864 hemophilia b 10.1
865 fragile x tremor/ataxia syndrome 10.1
866 sarcosinemia 10.1
867 lelis syndrome 10.1
868 chronic recurrent multifocal osteomyelitis 10.1
869 stargardt disease 10.1
870 kashin-beck disease 10.1
871 chronic inflammatory demyelinating polyneuropathy 10.1
872 dentinogenesis imperfecta 10.1
873 ectodermal dysplasia 10.1
874 hemangioma 10.1
875 tinea imbricata 10.1
876 maturity-onset diabetes of the young 10.1
877 brachydactyly 10.1
878 funisitis 10.1
879 polycystic liver disease 10.1
880 aphasia 10.1
881 simpson-golabi-behmel syndrome 10.1
882 persistent hyperplastic primary vitreous 10.1
883 peeling skin syndrome 10.1
884 left ventricular noncompaction 10.1
885 catecholaminergic polymorphic ventricular tachycardia 10.1
886 asbestosis 10.1
887 amblyopia 10.1
888 cystinosis 10.1
889 impulse control disorder 10.1
890 strongyloidiasis 10.1
891 spastic hemiplegia 10.1
892 hydronephrosis 10.1
893 horner's syndrome 10.1
894 emery-dreifuss muscular dystrophy 10.1
895 vaginal cancer 10.1
896 enterocele 10.1
897 hypochondriasis 10.1
898 periventricular leukomalacia 10.1
899 pernicious anemia 10.1
900 scleritis 10.1
901 generalized anxiety disorder 10.1
902 pyuria 10.1
903 hantavirus pulmonary syndrome 10.1
904 ventricular septal defect 10.1
905 vulvovaginitis 10.1
906 spondylolysis 10.1
907 nocardiosis 10.1
908 colon adenocarcinoma 10.1
909 relapsing polychondritis 10.1
910 pigmented villonodular synovitis 10.1
911 sertoli-leydig cell tumor 10.1
912 cutis laxa 10.1
913 pseudohypoparathyroidism 10.1
914 spindle cell sarcoma 10.1
915 akinetic mutism 10.1
916 multiple chemical sensitivity 10.1
917 hemangioblastoma 10.1
918 subacute thyroiditis 10.1
919 periapical periodontitis 10.1
920 pellagra 10.1
921 actinomycosis 10.1
922 night blindness 10.1
923 salivary gland cancer 10.1
924 pityriasis rosea 10.1
925 bronchiectasis 10.1
926 waterhouse-friderichsen syndrome 10.1
927 hyperphenylalaninemia 10.1
928 mutyh-associated polyposis 10.1
929 acanthamoeba keratitis 10.1
930 adolescent idiopathic scoliosis 10.1
931 angioimmunoblastic t-cell lymphoma 10.1
932 aplasia cutis congenita 10.1
933 asherman's syndrome 10.1
934 congenital rubella 10.1
935 cytomegalic inclusion disease 10.1
936 developmental prosopagnosia 10.1
937 diabetic mastopathy 10.1
938 diploid-triploid mosaicism 10.1
939 eisenmenger syndrome 10.1
940 glossodynia 10.1
941 hereditary neuropathy with liability to pressure palsy 10.1
942 human t-cell leukemia virus type 1 10.1
943 laugier-hunziker syndrome 10.1
944 pituitary stalk interruption syndrome 10.1
945 precocious puberty 10.1
946 recurrent respiratory papillomatosis 10.1
947 ring chromosome 20 10.1
948 serpiginous choroiditis 10.1
949 sirenomelia 10.1
950 sudden sensorineural hearing loss 10.1
951 syndrome of inappropriate antidiuretic hormone 10.1
952 triploidy 10.1
953 undifferentiated connective tissue disease 10.1
954 zika virus infection 10.1
955 combined pituitary hormone deficiency 10.1
956 sporadic hemiplegic migraine 10.1
957 febrile seizures 10.1
958 occipital neuralgia 10.1
959 spinal cord infarction 10.1
960 bickerstaff brainstem encephalitis 10.1
961 paraganglioma and gastric stromal sarcoma 10.1
962 glut1 deficiency syndrome 2, childhood onset 10.1
963 myelofibrosis with myeloid metaplasia, somatic 10.1
964 caudal regression syndrome 10.1
965 neu-laxova syndrome 1 10.1
966 fumarase deficiency 10.1
967 paroxysmal extreme pain disorder 10.1
968 donnai-barrow syndrome 10.1
969 hashimoto thyroiditis 10.1
970 hypocalcemia, autosomal dominant 10.1
971 cervical cancer, somatic 10.1
972 coach syndrome 10.1
973 hyaline fibromatosis syndrome 10.1
974 afibrinogenemia, congenital 10.1
975 factor xi deficiency, autosomal recessive 10.1
976 hartnup disorder 10.1
977 craniometaphyseal dysplasia 10.1
978 anencephaly 10.1
979 spastic paraplegia 72, autosomal recessive 10.1
980 craniometaphyseal dysplasia, autosomal recessive 10.1
981 osteopetrosis, autosomal recessive 5 10.1
982 metaphyseal chondrodysplasia, schmid type 10.1
983 rheumatoid arthritis, systemic juvenile 10.1
984 kaposi sarcoma 10.1
985 bile acid synthesis defect, congenital, 2 10.1
986 spastic paraplegia 18, autosomal recessive 10.1
987 osteopetrosis, autosomal recessive 3, with renal tubular acidosis 10.1
988 spastic paraplegia 8, autosomal dominant 10.1
989 hypomagnesemia 1, intestinal 10.1
990 fructose intolerance, hereditary 10.1
991 hirschsprung disease 1 10.1
992 wolman disease 10.1
993 mitochondrial dna depletion syndrome 7 10.1
994 porphyria, congenital erythropoietic 10.1
995 apert syndrome 10.1
996 costello syndrome 10.1
997 silver spastic paraplegia syndrome 10.1
998 osteopetrosis, autosomal dominant 1 10.1
999 osteopetrosis, autosomal recessive 1 10.1
1000 spastic paraplegia 10, autosomal dominant 10.1
1001 moebius syndrome 10.1
1002 peters-plus syndrome 10.1
1003 osteopetrosis, autosomal recessive 2 10.1
1004 hemifacial microsomia 10.1
1005 spastic paraplegia 49, autosomal recessive 10.1
1006 aortic valve disease 2 10.1
1007 mitochondrial dna depletion syndrome 4a 10.1
1008 osteopetrosis, autosomal recessive 4 10.1
1009 osteopetrosis, autosomal dominant 2 10.1
1010 liddle syndrome 10.1
1011 bile acid synthesis defect, congenital, 1 10.1
1012 brooke-spiegler syndrome 10.1
1013 spastic paraplegia 35, autosomal recessive 10.1
1014 malonyl-coa decarboxylase deficiency 10.1
1015 adenine phosphoribosyltransferase deficiency 10.1
1016 osteopetrosis, autosomal recessive 6 10.1
1017 caffey disease 10.1
1018 glanzmann thrombasthenia 10.1
1019 hyperkalemic periodic paralysis, type 2 10.1
1020 myotonia congenita, atypical, acetazolamide-responsive 10.1
1021 amyotrophy, hereditary neuralgic 10.1
1022 osteopetrosis, autosomal recessive 7 10.1
1023 cerebral creatine deficiency syndrome 2 10.1
1024 marshall-smith syndrome 10.1
1025 neurodegeneration with brain iron accumulation 3 10.1
1026 duane-radial ray syndrome 10.1
1027 osseous heteroplasia, progressive 10.1
1028 sneddon syndrome 10.1
1029 norrie disease 10.1
1030 renpenning syndrome 10.1
1031 hsd10 mitochondrial disease 10.1
1032 nystagmus 1, congenital, x-linked 10.1
1033 intestinal pseudoobstruction, neuronal 10.1
1034 myopathy, centronuclear, autosomal recessive 10.1
1035 piebaldism 10.1
1036 troyer syndrome 10.1
1037 myotubular myopathy, x-linked 10.1
1038 multiple enchondromatosis, maffucci type 10.1
1039 carney triad 10.1
1040 enchondromatosis, multiple, ollier type 10.1
1041 cerebellar hypoplasia 10.1
1042 chiari malformation type i 10.1
1043 x-linked sideroblastic anemia with ataxia 10.1
1044 hyperekplexia 10.1
1045 abducens nerve disease 10.1
1046 patulous eustachian tube 10.1
1047 congenital toxoplasmosis 10.1
1048 poems syndrome 10.1
1049 cystic kidney disease 10.1
1050 carbohydrate metabolic disorder 10.1
1051 lateral medullary syndrome 10.1
1052 von economo's disease 10.1
1053 paget's disease of bone 10.1
1054 molluscum contagiosum 10.1
1055 geniculate herpes zoster 10.1
1056 amino acid metabolic disorder 10.1
1057 genetic prion diseases 10.1
1058 glucose transporter type 1 deficiency syndrome 10.1
1059 mbd5 haploinsufficiency 10.1
1060 anophthalmos with limb anomalies 10.1
1061 cerulean cataract 10.1
1062 chronic hiccups 10.1
1063 dopa-responsive dystonia; segawa syndrome ad 10.1
1064 epilepsy occipital calcifications 10.1
1065 gigantomastia 10.1
1066 hemimegalencephaly 10.1
1067 kienbock's disease 10.1
1068 light chain deposition disease 10.1
1069 paroxysmal exertion-induced dyskinesia 10.1
1070 pepck 1 deficiency 10.1
1071 piriformis syndrome 10.1
1072 preauricular sinus 10.1
1073 primary orthostatic tremor 10.1
1074 scleredema 10.1
1075 sunct headache 10.1
1076 welander distal myopathy, swedish type 10.1
1077 central cord syndrome 10.1
1078 generalized gangliosidoses 10.1
1079 persistent vegetative state 10.1
1080 spastic paraplegia 78, autosomal recessive 10.0
1081 chromosome 1p36 deletion syndrome 10.0
1082 mitochondrial complex iv deficiency 10.0
1083 frontonasal dysplasia 1 10.0
1084 neuropathy, hereditary sensory and autonomic, type v 10.0
1085 lipodystrophy, familial partial, type 2 10.0
1086 porokeratosis 1, multiple types 10.0
1087 neuropathy, congenital hypomyelinating 10.0
1088 amelogenesis imperfecta, type ia 10.0
1089 spastic paraplegia 23 10.0
1090 gapo syndrome 10.0
1091 cataract 4, multiple types 10.0
1092 glomerulopathy with fibronectin deposits 2 10.0
1093 hyperoxaluria, primary, type 1 10.0
1094 ulna and fibula, absence of, with severe limb deficiency 10.0
1095 muscular dystrophy-dystroglycanopathy , type c, 14 10.0
1096 atelosteogenesis, type i 10.0
1097 orotic aciduria 10.0
1098 keratosis, seborrheic, somatic 10.0
1099 optic atrophy 1 10.0
1100 spastic paraplegia 79, autosomal recessive 10.0
1101 amelogenesis imperfecta, type if 10.0
1102 migraine with or without aura 1 10.0
1103 pseudohypoaldosteronism type i, autosomal dominant 10.0
1104 glutaric acidemia iic 10.0
1105 dyskeratosis, hereditary benign intraepithelial 10.0
1106 d-bifunctional protein deficiency 10.0
1107 chylomicron retention disease 10.0
1108 myofibromatosis, infantile, 1 10.0
1109 netherton syndrome 10.0
1110 ventricular septal defect 3 10.0
1111 macrocephaly/megalencephaly syndrome, autosomal recessive 10.0
1112 ventricular septal defect 2 10.0
1113 spastic paraplegia 48, autosomal recessive 10.0
1114 spondylocostal dysostosis 3, autosomal recessive 10.0
1115 saethre-chotzen syndrome 10.0
1116 pallister-hall syndrome 10.0
1117 silver-russell syndrome 10.0
1118 dihydrolipoamide dehydrogenase deficiency 10.0
1119 thiamine metabolism dysfunction syndrome 5 10.0
1120 ventricular septal defect 1 10.0
1121 roberts syndrome 10.0
1122 spastic paraplegia 5a, autosomal recessive 10.0
1123 klippel-trenaunay-weber syndrome 10.0
1124 ritscher-schinzel syndrome 1 10.0
1125 verheij syndrome 10.0
1126 amyotrophic lateral sclerosis 14, with or without frontotemporal dementia 10.0
1127 fructose-1,6-bisphosphatase deficiency 10.0
1128 spinal muscular atrophy, lower extremity-predominant, 2, ad 10.0
1129 charcot-marie-tooth disease, axonal, type 2p 10.0
1130 urofacial syndrome 1 10.0
1131 crouzon syndrome 10.0
1132 gyrate atrophy of choroid and retina with or without ornithinemia 10.0
1133 mcardle disease 10.0
1134 albinism, oculocutaneous, type ib 10.0
1135 ichthyosis bullosa of siemens 10.0
1136 fibrosis of extraocular muscles, congenital, 1 10.0
1137 achalasia-addisonianism-alacrimia syndrome 10.0
1138 epidermolytic hyperkeratosis 10.0
1139 monilethrix 10.0
1140 spondyloepiphyseal dysplasia tarda, autosomal dominant 10.0
1141 stickler syndrome, type i 10.0
1142 legg-calve-perthes disease 10.0
1143 glycogen storage disease vii 10.0
1144 deafness and myopia 10.0
1145 spastic paraplegia 3a, autosomal dominant 10.0
1146 thyroid cancer, nonmedullary, 1 10.0
1147 chorea, hereditary benign 10.0
1148 chromosome 15q11.2 deletion syndrome 10.0
1149 isovaleric acidemia 10.0
1150 mast syndrome 10.0
1151 reticulate acropigmentation of kitamura 10.0
1152 galloway-mowat syndrome 10.0
1153 epilepsy, focal, with speech disorder and with or without mental retardation 10.0
1154 epileptic encephalopathy, early infantile, 17 10.0
1155 fibrosis of extraocular muscles, congenital, 3a 10.0
1156 adrenal cortical carcinoma 10.0
1157 steatocystoma multiplex 10.0
1158 supranuclear palsy, progressive 10.0
1159 n-acetylglutamate synthase deficiency 10.0
1160 peroxisomal acyl-coa oxidase deficiency 10.0
1161 glutaricaciduria, type i 10.0
1162 cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 10.0
1163 prolidase deficiency 10.0
1164 dystonia-12 10.0
1165 central core disease 10.0
1166 sea-blue histiocyte disease 10.0
1167 spastic paraplegia 12, autosomal dominant 10.0
1168 waardenburg syndrome, type 2e, with or without neurologic involvement 10.0
1169 infantile neuroaxonal dystrophy 1 10.0
1170 nystagmus 6, congenital, x-linked 10.0
1171 coffin-lowry syndrome 10.0
1172 nance-horan syndrome 10.0
1173 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 10.0
1174 spastic paraplegia 2, x-linked 10.0
1175 mental retardation, x-linked 3 10.0
1176 masa syndrome 10.0
1177 microphthalmia, syndromic 1 10.0
1178 trifunctional protein deficiency 10.0
1179 polyposis, juvenile intestinal 10.0
1180 chromosome 15q13.3 microdeletion syndrome 10.0
1181 choroid plexus papilloma 10.0
1182 cone-rod dystrophy 10.0
1183 rabson-mendenhall syndrome 10.0
1184 kearns-sayre syndrome 10.0
1185 ebstein anomaly 10.0
1186 emphysema, congenital lobar 10.0
1187 chiari malformation type ii 10.0
1188 lipomatosis, multiple symmetric 10.0
1189 valproate embryopathy, susceptibility to 10.0
1190 melorheostosis, isolated 10.0
1191 isotretinoin embryopathy-like syndrome 10.0
1192 satoyoshi syndrome 10.0
1193 sprengel deformity 10.0
1194 pulmonary alveolar proteinosis, acquired 10.0
1195 coronary artery dissection, spontaneous 10.0
1196 angel-shaped phalangoepiphyseal dysplasia 10.0
1197 marcus gunn phenomenon 10.0
1198 blue diaper syndrome 10.0
1199 letterer-siwe disease 10.0
1200 sydenham chorea 10.0
1201 childhood type dermatomyositis 10.0
1202 dengue disease 10.0
1203 myelodysplastic myeloproliferative cancer 10.0
1204 systemic scleroderma 10.0
1205 aicardi-goutieres syndrome 10.0
1206 primary cutaneous amyloidosis 10.0
1207 persistent mullerian duct syndrome 10.0
1208 ileocolitis 10.0
1209 porencephaly 10.0
1210 primary hypomagnesemia 10.0
1211 ossification of the posterior longitudinal ligament of spine 10.0
1212 fibrous dysplasia 10.0
1213 sialadenitis 10.0
1214 spermatic cord torsion 10.0
1215 conn's syndrome 10.0
1216 dieulafoy lesion 10.0
1217 coloboma 10.0
1218 balantidiasis 10.0
1219 vulva cancer 10.0
1220 locked-in syndrome 10.0
1221 multiple epiphyseal dysplasia 10.0
1222 pars planitis 10.0
1223 typhoid fever 10.0
1224 tinea manuum 10.0
1225 urethral syndrome 10.0
1226 geographic tongue 10.0
1227 acrodysostosis 10.0
1228 congenital ichthyosiform erythroderma 10.0
1229 optic nerve disease 10.0
1230 fallopian tube carcinoma 10.0
1231 syringoma 10.0
1232 west nile encephalitis 10.0
1233 lymphangiosarcoma 10.0
1234 glucosephosphate dehydrogenase deficiency 10.0
1235 neurilemmoma 10.0
1236 uterine disease 10.0
1237 gorham's disease 10.0
1238 acral lentiginous melanoma 10.0
1239 47,xyy syndrome 10.0
1240 arsacs 10.0
1241 cask-related disorders 10.0
1242 peroxisome biogenesis disorders, zellweger syndrome spectrum 10.0
1243 y chromosome infertility 10.0
1244 acute flaccid myelitis 10.0
1245 acute necrotizing encephalopathy 10.0
1246 antisynthetase syndrome 10.0
1247 autoimmune atrophic gastritis 10.0
1248 cerebellar degeneration 10.0
1249 cockayne syndrome type ii 10.0
1250 colpocephaly 10.0
1251 congenital analbuminemia 10.0
1252 congenital laryngeal palsy 10.0
1253 congenital varicella syndrome 10.0
1254 corpus callosum agenesis 10.0
1255 early-onset generalized dystonia 10.0
1256 erythema nodosum, idiopathic 10.0
1257 familial progressive cardiac conduction defect 10.0
1258 gianotti crosti syndrome 10.0
1259 granulomatous rosacea 10.0
1260 harlequin syndrome 10.0
1261 hemihypertrophy 10.0
1262 htlv-1 associated myelopathy/tropical spastic paraparesis 10.0
1263 ichthyosis follicularis atrichia photophobia syndrome 10.0
1264 idiopathic hypersomnia 10.0
1265 igg4-related disease 10.0
1266 immunoglobulin g deficiency 10.0
1267 laryngeal papillomatosis 10.0
1268 levator syndrome 10.0
1269 maculopapular cutaneous mastocytosis 10.0
1270 mitochondrial complex iii deficiency 10.0
1271 mondini dysplasia 10.0
1272 myosin storage myopathy 10.0
1273 not otherwise specified 3-mga-uria type 10.0
1274 oligomeganephronic renal hypoplasia 10.0
1275 ovarian remnant syndrome 10.0
1276 paroxysmal cold hemoglobinuria 10.0
1277 pseudoangiomatous stromal hyperplasia 10.0
1278 pseudopelade of brocq 10.0
1279 renal tubular acidosis, distal 10.0
1280 rosai-dorfman disease 10.0
1281 small intestinal adenocarcinoma 10.0
1282 urachal cyst 10.0
1283 woolly hair syndrome 10.0
1284 wyburn mason's syndrome 10.0
1285 central cervical cord syndrome 10.0
1286 cerebral atrophy 10.0
1287 hemifacial spasm 10.0
1288 hemiplegia alterans 10.0
1289 meningitis and encephalitis 10.0
1290 myoclonic encephalopathy of infants 10.0
1291 apnea of prematurity 10.0
1292 prostatitis 10.0
1293 corneal dystrophy, schnyder type 10.0
1294 immunodeficiency due to ficolin 3 deficiency 10.0
1295 erythrokeratodermia variabilis et progressiva 1 10.0
1296 methylmalonic aciduria and homocystinuria, cblc type 10.0
1297 epileptic encephalopathy, early infantile, 15 10.0
1298 basal cell nevus syndrome 10.0
1299 dihydropyrimidine dehydrogenase deficiency 10.0
1300 stickler syndrome, type ii 10.0
1301 spastic paraplegia 63 10.0
1302 thrombocytopenia-absent radius syndrome 10.0
1303 urbach-wiethe disease 10.0
1304 ichthyosis vulgaris 10.0
1305 gaucher disease, type i 10.0
1306 migraine, familial hemiplegic, 2 10.0
1307 cataract 1, multiple types 10.0
1308 dejerine-sottas disease 10.0
1309 hyperlipidemia, familial combined 10.0
1310 macular degeneration, age-related, 1 10.0
1311 nystagmus 7, congenital, autosomal dominant 10.0
1312 chromosome 1q41-q42 deletion syndrome 10.0
1313 nemaline myopathy 3, autosomal dominant or recessive 10.0
1314 spastic paraplegia 44, autosomal recessive 10.0
1315 spastic paraplegia 74, autosomal recessive 10.0
1316 muckle-wells syndrome 10.0
1317 cinca syndrome 10.0
1318 mental retardation, autosomal dominant 22 10.0
1319 anterior segment dysgenesis 7, with sclerocornea 10.0
1320 mismatch repair cancer syndrome 10.0
1321 spastic paraplegia 4, autosomal dominant 10.0
1322 diarrhea 5, with tufting enteropathy, congenital 10.0
1323 spastic paraplegia 31, autosomal dominant 10.0
1324 whim syndrome 10.0
1325 migraine, familial hemiplegic, 3 10.0
1326 tumoral calcinosis, hyperphosphatemic, familial 10.0
1327 myasthenic syndrome, congenital, 1a, slow-channel 10.0
1328 vertical talus, congenital 10.0
1329 myasthenic syndrome, congenital, 3a, slow-channel 10.0
1330 cerebrotendinous xanthomatosis 10.0
1331 spastic paraplegia 13, autosomal dominant 10.0
1332 ichthyosis, congenital, autosomal recessive 4a 10.0
1333 carbamoylphosphate synthetase i deficiency 10.0
1334 centronuclear myopathy 5 10.0
1335 thiamine metabolism dysfunction syndrome 2 10.0
1336 bethlem myopathy 1 10.0
1337 spastic paraplegia 30, autosomal recessive 10.0
1338 neuropathy, hereditary sensory and autonomic, type vii 10.0
1339 septooptic dysplasia 10.0
1340 chanarin-dorfman syndrome 10.0
1341 atelosteogenesis, type iii 10.0
1342 blepharophimosis, epicanthus inversus, and ptosis, type 1 10.0
1343 spastic paraplegia 42, autosomal dominant 10.0
1344 encephalopathy, familial, with neuroserpin inclusion bodies 10.0
1345 hypotrichosis 7 10.0
1346 ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis 10.0
1347 behr syndrome 10.0
1348 fraser syndrome 1 10.0
1349 spastic paraplegia 56, autosomal recessive 10.0
1350 chondrocalcinosis 2 10.0
1351 amyloidosis, primary localized cutaneous, 1 10.0
1352 amyloidosis, primary localized cutaneous, 2 10.0
1353 pseudo-torch syndrome 1 10.0
1354 parkes weber syndrome 10.0
1355 pancreatitis, hereditary 10.0
1356 treacher collins syndrome 1 10.0
1357 ichthyosis, congenital, autosomal recessive 6 10.0
1358 spastic paraplegia 77, autosomal recessive 10.0
1359 succinic semialdehyde dehydrogenase deficiency 10.0
1360 antiphospholipid syndrome, familial 10.0
1361 ichthyosis, congenital, autosomal recessive 10 10.0
1362 3-m syndrome 1 10.0
1363 nystagmus 2, congenital, autosomal dominant 10.0
1364 macular dystrophy, north carolina type 10.0
1365 yunis-varon syndrome 10.0
1366 spastic paraplegia and psychomotor retardation with or without seizures 10.0
1367 argininemia 10.0
1368 plasminogen deficiency, type i 10.0
1369 chordoma 10.0
1370 dystonia, juvenile-onset 10.0
1371 leukodystrophy, hypomyelinating, 5 10.0
1372 mody, type ii 10.0
1373 diabetes mellitus, permanent neonatal 10.0
1374 wilms tumor susceptibility-5 10.0
1375 hypothalamic hamartomas, somatic 10.0
1376 nystagmus 3, congenital, autosomal dominant 10.0
1377 supravalvar aortic stenosis 10.0
1378 cutis laxa, autosomal dominant 10.0
1379 cholestasis, progressive familial intrahepatic 3 10.0
1380 citrullinemia, adult-onset type ii 10.0
1381 spastic paraplegia 50, autosomal recessive 10.0
1382 weaver syndrome 10.0
1383 single median maxillary central incisor 10.0
1384 keratolytic winter erythema 10.0
1385 squamous cell carcinoma, head and neck 10.0
1386 hypermanganesemia with dystonia 2 10.0
1387 pfeiffer syndrome 10.0
1388 jackson-weiss syndrome 10.0
1389 nijmegen breakage syndrome 10.0
1390 brown-vialetto-van laere syndrome 2 10.0
1391 polycythemia vera, somatic 10.0
1392 myasthenic syndrome, congenital, 14, with tubular aggregates 10.0
1393 porphyria, acute hepatic 10.0
1394 genitopatellar syndrome 10.0
1395 myopathy with extrapyramidal signs 10.0
1396 ichthyosis, congenital, autosomal recessive 8 10.0
1397 dubin-johnson syndrome 10.0
1398 spastic paraplegia 64, autosomal recessive 10.0
1399 meningioma, familial 10.0
1400 spastic paraplegia 33, autosomal dominant 10.0
1401 spastic paraplegia 9a, autosomal dominant 10.0
1402 spastic paraplegia 9b, autosomal recessive 10.0
1403 spastic paraplegia 45, autosomal recessive 10.0
1404 spastic paraplegia 62 10.0
1405 anterior segment dysgenesis 1, multiple subtypes 10.0
1406 peroxisome biogenesis disorder 8b 10.0
1407 smith-lemli-opitz syndrome 10.0
1408 spastic paraplegia, optic atrophy, and neuropathy 10.0
1409 spastic paraplegia 76, autosomal recessive 10.0
1410 aicardi-goutieres syndrome 3 10.0
1411 pituitary adenoma, prolactin-secreting 10.0
1412 periodontitis 1, juvenile 10.0
1413 hypomagnesemia 2, renal 10.0
1414 glycogen storage disease ib 10.0
1415 ichthyosis, congenital, autosomal recessive 11 10.0
1416 isobutyryl-coa dehydrogenase deficiency 10.0
1417 periodic fever, familial 10.0
1418 pseudohypoaldosteronism, type i 10.0
1419 ichthyosis, congenital, autosomal recessive 7 10.0
1420 ichthyosis histrix, curth-macklin type 10.0
1421 myxoid liposarcoma 10.0
1422 spastic paraplegia 26, autosomal recessive 10.0
1423 myopathy, centronuclear, 3 10.0
1424 mucolipidosis iii alpha/beta 10.0
1425 brachyolmia type 3 10.0
1426 diabetes mellitus, insulin-dependent 10.0
1427 cataract 14, multiple types 10.0
1428 wilson disease 10.0
1429 nystagmus 4, congenital, autosomal dominant 10.0
1430 catel-manzke syndrome 10.0
1431 ichthyosis, congenital, autosomal recessive 1 10.0
1432 spastic paraplegia 28, autosomal recessive 10.0
1433 microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma 10.0
1434 spastic paraplegia 15, autosomal recessive 10.0
1435 nevus comedonicus, somatic 10.0
1436 proteus syndrome, somatic 10.0
1437 spastic paraplegia 6, autosomal dominant 10.0
1438 lung disease, immunodeficiency, and chromosome breakage syndrome 10.0
1439 legius syndrome 10.0
1440 johanson-blizzard syndrome 10.0
1441 spastic paraplegia 11, autosomal recessive 10.0
1442 ichthyosis, congenital, autosomal recessive 9 10.0
1443 thalassemias, alpha- 10.0
1444 myopathy, centronuclear, 4 10.0
1445 ceroid lipofuscinosis, neuronal, 3 10.0
1446 brody myopathy 10.0
1447 spastic paraplegia 61, autosomal recessive 10.0
1448 spondylocostal dysostosis 5 10.0
1449 cylindromatosis, familial 10.0
1450 macular corneal dystrophy 10.0
1451 cataract 21, multiple types 10.0
1452 tyrosinemia, type ii 10.0
1453 fanconi anemia, complementation group a 10.0
1454 lymphedema-distichiasis syndrome 10.0
1455 spastic paraplegia 7, autosomal recessive 10.0
1456 ichthyosis, congenital, autosomal recessive 2 10.0
1457 ichthyosis, congenital, autosomal recessive 3 10.0
1458 myasthenic syndrome, congenital, 4a, slow-channel 10.0
1459 myasthenic syndrome, congenital, 2a, slow-channel 10.0
1460 folate malabsorption, hereditary 10.0
1461 cataract 10, multiple types 10.0
1462 neurofibromatosis, familial spinal 10.0
1463 growth hormone insensitivity with immunodeficiency 10.0
1464 koolen-de vries syndrome 10.0
1465 tarsal-carpal coalition syndrome 10.0
1466 pierre robin syndrome 10.0
1467 campomelic dysplasia 10.0
1468 amyloidosis, hereditary, transthyretin-related 10.0
1469 carpal tunnel syndrome, familial 10.0
1470 myhre syndrome 10.0
1471 lipodystrophy, partial, acquired 10.0
1472 spastic paraplegia 39, autosomal recessive 10.0
1473 leukodystrophy, hypomyelinating, 6 10.0
1474 myofibromatosis, infantile 2 10.0
1475 ichthyosis, congenital, autosomal recessive 5 10.0
1476 migraine, familial hemiplegic, 1 10.0
1477 right atrial isomerism 10.0
1478 neurodegeneration with brain iron accumulation 4 10.0
1479 spastic paraplegia 43, autosomal recessive 10.0
1480 spastic paraplegia 75, autosomal recessive 10.0
1481 minicore myopathy with external ophthalmoplegia 10.0
1482 camurati-engelmann disease 10.0
1483 spastic paraplegia 73, autosomal dominant 10.0
1484 brown-vialetto-van laere syndrome 1 10.0
1485 neurodegeneration with brain iron accumulation 1 10.0
1486 corneal endothelial dystrophy and perceptive deafness 10.0
1487 thrombophilia due to thrombomodulin defect 10.0
1488 brachydactyly, type c 10.0
1489 glutathione synthetase deficiency 10.0
1490 arterial tortuosity syndrome 10.0
1491 mccune-albright syndrome, somatic, mosaic 10.0
1492 tukel syndrome 10.0
1493 amyotrophic lateral sclerosis 1 10.0
1494 holoprosencephaly 1 10.0
1495 velocardiofacial syndrome 10.0
1496 cataract 3, multiple types 10.0
1497 cataract 23 10.0
1498 leukemia, chronic myeloid, somatic 10.0
1499 schwannomatosis 10.0
1500 epilepsy, familial focal, with variable foci 1 10.0
1501 langer mesomelic dysplasia 10.0
1502 ichthyosis, x-linked 10.0
1503 orofaciodigital syndrome i 10.0
1504 pyruvate dehydrogenase e1-alpha deficiency 10.0
1505 nystagmus 5, congenital, x-linked 10.0
1506 focal dermal hypoplasia 10.0
1507 hypophosphatemic rickets 10.0
1508 leber optic atrophy 10.0
1509 androgen insensitivity, partial, with or without breast cancer 10.0
1510 osteopathia striata with cranial sclerosis 10.0
1511 premature ovarian failure 1 10.0
1512 melnick-needles syndrome 10.0
1513 mucopolysaccharidosis ii 10.0
1514 blue cone monochromacy 10.0
1515 hmg-coa lyase deficiency 10.0
1516 uncombable hair syndrome 10.0
1517 lchad deficiency 10.0
1518 brachydactyly, type e 10.0
1519 hip dysplasia, beukes type 10.0
1520 carpenter syndrome 10.0
1521 ectodermal dysplasia 2, clouston type 10.0
1522 dyserythropoietic anemia, congenital, type iii 10.0
1523 olmsted syndrome 10.0
1524 insomnia, fatal familial 10.0
1525 chromosome 22q11.2 microduplication syndrome 10.0
1526 mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes 10.0
1527 pearson marrow-pancreas syndrome 10.0
1528 duodenal atresia 10.0
1529 oculocerebrocutaneous syndrome 10.0
1530 gomez-lopez-hernandez syndrome 10.0
1531 fryns syndrome 10.0
1532 femoral-facial syndrome 10.0
1533 split-foot deformity with mandibulofacial dysostosis 10.0
1534 autoimmune polyendocrine syndrome, type ii 10.0
1535 corpus callosum, agenesis of, with facial anomalies and robin sequence 10.0
1536 deafness, progressive, with stapes fixation 10.0
1537 angioma, tufted 10.0
1538 histidinemia 10.0
1539 ringed hair 10.0
1540 chronic kidney failure 10.0
1541 diamond-blackfan anemia 10.0
1542 epidermolysis bullosa dystrophica 10.0
1543 leber congenital amaurosis 10.0
1544 lymphomatoid granulomatosis 10.0
1545 osteochondritis dissecans 10.0
1546 lambert-eaton myasthenic syndrome 10.0
1547 loeys-dietz syndrome 10.0
1548 asphyxiating thoracic dystrophy 10.0
1549 familial atrial fibrillation 10.0
1550 3-methylcrotonyl-coa carboxylase deficiency 10.0
1551 townes-brocks syndrome 10.0
1552 juvenile absence epilepsy 10.0
1553 familial hemiplegic migraine 10.0
1554 lymphocytic colitis 10.0
1555 crest syndrome 10.0
1556 stuttering 10.0
1557 tracheomalacia 10.0
1558 umbilical hernia 10.0
1559 cole-carpenter syndrome 10.0
1560 split hand-foot malformation 10.0
1561 split hand-foot malformation 1 10.0
1562 paralytic squint 10.0
1563 lipoid nephrosis 10.0
1564 henoch-schoenlein purpura 10.0
1565 fuchs' endothelial dystrophy 10.0
1566 frey syndrome 10.0
1567 cortical blindness 10.0
1568 panuveitis 10.0
1569 entropion 10.0
1570 tinea pedis 10.0
1571 trichuriasis 10.0
1572 blastomycosis 10.0
1573 corpus luteum cyst 10.0
1574 acute cystitis 10.0
1575 loiasis 10.0
1576 neuroschistosomiasis 10.0
1577 46 xy gonadal dysgenesis 10.0
1578 vacterl association 10.0
1579 axenfeld-rieger syndrome 10.0
1580 olivopontocerebellar atrophy 10.0
1581 blount's disease 10.0
1582 disease of mental health 10.0
1583 conversion disorder 10.0
1584 gestational choriocarcinoma 10.0
1585 factor xiii deficiency 10.0
1586 west nile fever 10.0
1587 gangliocytoma 10.0
1588 blepharoconjunctivitis 10.0
1589 iga glomerulonephritis 10.0
1590 grade iii astrocytoma 10.0
1591 lipid metabolism disorder 10.0
1592 toxic encephalopathy 10.0
1593 adrenal carcinoma 10.0
1594 ascariasis 10.0
1595 gerstmann syndrome 10.0
1596 myxopapillary ependymoma 10.0
1597 strabismus 10.0
1598 peripheral nervous system disease 10.0
1599 bronchitis 10.0
1600 monoclonal gammopathy of uncertain significance 10.0
1601 malignant spiradenoma 10.0
1602 brachial plexus lesion 10.0
1603 intestinal volvulus 10.0
1604 perinatal necrotizing enterocolitis 10.0
1605 pyomyositis 10.0
1606 evans' syndrome 10.0
1607 sideroblastic anemia 10.0
1608 amebiasis 10.0
1609 hemorrhoid 10.0
1610 albinism 10.0
1611 biotin-thiamine-responsive basal ganglia disease 10.0
1612 familial paroxysmal kinesigenic dyskinesia 10.0
1613 myofibrillar myopathy 10.0
1614 nuclear gene-encoded leigh syndrome 10.0
1615 primary familial brain calcification 10.0
1616 48,xxxy syndrome 10.0
1617 abdominal cystic lymphangioma 10.0
1618 accessory navicular bone 10.0
1619 acroosteolysis dominant type 10.0
1620 acute zonal occult outer retinopathy 10.0
1621 adult-onset immunodeficiency with anti-interferon-gamma autoantibodies 10.0
1622 al amyloidosis 10.0
1623 alezzandrini syndrome 10.0
1624 anonychia-onychodystrophy with hypoplasia or absence of distal phalanges 10.0
1625 autosomal dominant intellectual disability 30 10.0
1626 bamforth syndrome 10.0
1627 baroreflex failure 10.0
1628 bednar tumor 10.0
1629 black hairy tongue 10.0
1630 broken heart syndrome 10.0
1631 brown syndrome 10.0
1632 central congenital hypothyroidism 10.0
1633 cerebro-oculo-facio-skeletal syndrome 10.0
1634 chaotic atrial tachycardia 10.0
1635 childhood hepatocellular carcinoma 10.0
1636 chromosome 10p deletion 10.0
1637 chronic active epstein-barr virus infection 10.0
1638 chronic intestinal pseudoobstruction 10.0
1639 de barsy syndrome 10.0
1640 desmoplastic small round cell tumor 10.0
1641 diffuse dermal angiomatosis 10.0
1642 diffuse idiopathic pulmonary neuroendocrine cell hyperplasia 10.0
1643 digestive system melanoma 10.0
1644 disseminated peritoneal leiomyomatosis 10.0
1645 dysfibrinogenemia 10.0
1646 eagle syndrome 10.0
1647 epidermoid brain tumor 10.0
1648 exercise-induced anaphylaxis 10.0
1649 extracranial arteriovenous malformation 10.0
1650 familial osteochondritis dissecans 10.0
1651 fibro-adipose vascular anomaly 10.0
1652 fibrosing mediastinitis 10.0
1653 foxg1 syndrome 10.0
1654 genuine diffuse phlebectasia 10.0
1655 giant congenital nevus 10.0
1656 heavy metal poisoning 10.0
1657 hereditary geniospasm 10.0
1658 herpes simplex encephalitis 10.0
1659 hypertrophic olivary degeneration 10.0
1660 idiopathic hypertrophic pachymeningitis 10.0
1661 iqsec2 10.0
1662 isolated ectopia lentis 10.0
1663 juvenile amyotrophic lateral sclerosis 10.0
1664 juvenile spondyloarthropathy 10.0
1665 klumpke paralysis 10.0
1666 lewis-sumner syndrome 10.0
1667 lichen planopilaris 10.0
1668 ligneous conjunctivitis 10.0
1669 lipedematous scalp 10.0
1670 localized lipodystrophy 10.0
1671 lymphatic malformations 10.0
1672 madelung deformity 10.0
1673 malignant migrating partial seizures of infancy 10.0
1674 mannose-binding lectin protein deficiency 10.0
1675 metatarsus adductus 10.0
1676 migraine with brainstem aura 10.0
1677 mounier-kuhn syndrome 10.0
1678 multiple familial trichoepithelioma 10.0
1679 murcs association 10.0
1680 muscular phosphorylase kinase deficiency 10.0
1681 non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 10.0
1682 noonan-like/multiple giant cell lesion syndrome 10.0
1683 ophn1 syndrome 10.0
1684 oral leukoplakia 10.0
1685 ovarian sex cord tumor with annular tubules 10.0
1686 painful legs and moving toes syndrome 10.0
1687 persistent genital arousal disorder 10.0
1688 phace syndrome 10.0
1689 phocomelia 10.0
1690 phosphoglycerate kinase deficiency 10.0
1691 pigmented purpuric dermatosis 10.0
1692 pili torti 10.0
1693 pineal cyst 10.0
1694 pityriasis lichenoides et varioliformis acuta 10.0
1695 primary orthostatic hypotension 10.0
1696 proliferating trichilemmal cyst 10.0
1697 propriospinal myoclonus 10.0
1698 pulmonary arterio-veinous fistula 10.0
1699 pure autonomic failure 10.0
1700 pustulosis palmaris et plantaris 10.0
1701 rasmussen encephalitis 10.0
1702 renal nutcracker syndrome 10.0
1703 riboflavin transporter deficiency 10.0
1704 satb2-associated syndrome 10.0
1705 scn2a related disorders 10.0
1706 split hand split foot malformation autosomal recessive 10.0
1707 split hand/foot malformation x-linked 10.0
1708 streptococcal group a invasive disease 10.0
1709 superficial siderosis of the central nervous system 10.0
1710 swyer-james syndrome 10.0
1711 systemic capillary leak syndrome 10.0
1712 thrombotic thrombocytopenic purpura, acquired 10.0
1713 thyroid cancer, anaplastic 10.0
1714 trigeminal trophic syndrome 10.0
1715 trochleitis 10.0
1716 urachal cancer 10.0
1717 visual snow syndrome 10.0
1718 wagner syndrome 10.0
1719 wandering spleen 10.0
1720 warm antibody hemolytic anemia 10.0
1721 warthin tumor 10.0
1722 zlotogora syndrome 10.0
1723 aldosterone-producing adenoma 10.0
1724 central precocious puberty 10.0
1725 cumulative trauma disorders 10.0
1726 de morsier's syndrome information 10.0
1727 developmental dyspraxia 10.0
1728 erb's palsy 10.0
1729 familial periodic paralyses 10.0
1730 immune-mediated encephalomyelitis 10.0
1731 lyme disease - neurological complications 10.0
1732 mucopolysaccharidoses 10.0
1733 o'sullivan-mcleod syndrome 10.0
1734 overuse syndrome 10.0
1735 periodic paralyses 10.0
1736 pinched nerve 10.0
1737 postinfectious encephalomyelitis 10.0
1738 repetitive motion disorders 10.0
1739 repetitive stress injuries 10.0
1740 cleft lip/palate 10.0
1741 ethylene glycol poisoning 10.0
1742 endotheliitis 9.9
1743 thyroiditis 9.9
1744 masp2 deficiency 9.9
1745 schwartz-jampel syndrome, type 1 9.9
1746 cerebellar ataxia, nonprogressive, with mental retardation 9.9
1747 bartter syndrome, type 4b, digenic 9.9
1748 galactose epimerase deficiency 9.9
1749 dystonia 9 9.9
1750 glycine encephalopathy with normal serum glycine 9.9
1751 parkinson disease 19a, juvenile-onset 9.9
1752 breasts and/or nipples, aplasia or hypoplasia of, 2 9.9
1753 inflammatory bowel disease 17, protection against 9.9
1754 bartter syndrome, type 4a 9.9
1755 mesothelioma, somatic 9.9
1756 glycogen storage disease iiia 9.9
1757 schimmelpenning-feuerstein-mims syndrome, somatic mosaic 9.9
1758 cousin syndrome 9.9
1759 myopathy, vacuolar, with casq1 aggregates 9.9
1760 renal cell carcinoma, papillary 9.9
1761 insensitivity to pain, congenital, with anhidrosis 9.9
1762 chromosome 1q21.1 duplication syndrome 9.9
1763 mandibuloacral dysplasia 9.9
1764 porphyria variegata 9.9
1765 thrombocytopenic purpura, autoimmune 9.9
1766 mitochondrial complex i deficiency 9.9
1767 trimethylaminuria 9.9
1768 giant axonal neuropathy 2, autosomal dominant 9.9
1769 muscular dystrophy, limb-girdle, type 2y 9.9
1770 hyperparathyroidism, familial primary 9.9
1771 graft-versus-host disease, protection against 9.9
1772 ataxia, posterior column, with retinitis pigmentosa 9.9
1773 basal laminar drusen 9.9
1774 prune belly syndrome 9.9
1775 reynolds syndrome 9.9
1776 megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 9.9
1777 familial cold-induced inflammatory syndrome 1 9.9
1778 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 2 9.9
1779 feingold syndrome 1 9.9
1780 hypobetalipoproteinemia 9.9
1781 shashi-pena syndrome 9.9
1782 myoglobinuria, acute recurrent, autosomal recessive 9.9
1783 cystinuria 9.9
1784 miyoshi muscular dystrophy 1 9.9
1785 perry syndrome 9.9
1786 ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive 9.9
1787 thrombophilia due to protein c deficiency, autosomal recessive 9.9
1788 hypomyelination with brainstem and spinal cord involvement and leg spasticity 9.9
1789 mowat-wilson syndrome 9.9
1790 woodhouse-sakati syndrome 9.9
1791 fibrodysplasia ossificans progressiva 9.9
1792 cholestasis, progressive familial intrahepatic 2 9.9
1793 aicardi-goutieres syndrome 7 9.9
1794 epileptic encephalopathy, early infantile, 6 9.9
1795 erythermalgia, primary 9.9
1796 amelogenesis imperfecta, type ih 9.9
1797 hemochromatosis, type 4 9.9
1798 ehlers-danlos syndrome, type iv 9.9
1799 mitochondrial complex iii deficiency, nuclear type 1 9.9
1800 pulmonary venoocclusive disease 1 9.9
1801 schimke immunoosseous dysplasia 9.9
1802 hypotonia, infantile, with psychomotor retardation and characteristic facies 2 9.9
1803 dyschromatosis universalis hereditaria 3 9.9
1804 alport syndrome, autosomal recessive 9.9
1805 pseudohypoaldosteronism, type iie 9.9
1806 specific language impairment 5 9.9
1807 ullrich congenital muscular dystrophy 1 9.9
1808 hyperbilirubinemia, familial transient neonatal 9.9
1809 inflammatory bowel disease 10 9.9
1810 intellectual developmental disorder with dysmorphic facies and ptosis 9.9
1811 nail disorder, nonsyndromic congenital, 3, 9.9
1812 gm1-gangliosidosis, type i 9.9
1813 gm1-gangliosidosis, type ii 9.9
1814 gm1-gangliosidosis, type iii 9.9
1815 mucopolysaccharidosis type ivb 9.9
1816 muscular dystrophy-dystroglycanopathy , type b, 14 9.9
1817 nephrotic syndrome, type 5, with or without ocular abnormalities 9.9
1818 pierson syndrome 9.9
1819 cholangitis, primary sclerosing 9.9
1820 heart block, progressive, type ia 9.9
1821 larsen syndrome 9.9
1822 boomerang dysplasia 9.9
1823 tietz albinism-deafness syndrome 9.9
1824 melanoma, cutaneous malignant 8 9.9
1825 vesicoureteral reflux 2 9.9
1826 coproporphyria 9.9
1827 immunodeficiency 21 9.9
1828 leukemia, acute myeloid 9.9
1829 propionicacidemia 9.9
1830 leukoencephalopathy with ataxia 9.9
1831 fanconi-bickel syndrome 9.9
1832 megalencephaly-capillary malformation-polymicrogyria syndrome, somatic 9.9
1833 limb-mammary syndrome 9.9
1834 epileptic encephalopathy, early infantile, 47 9.9
1835 hypochondroplasia 9.9
1836 fetal akinesia deformation sequence 9.9
1837 spondylo-megaepiphyseal-metaphyseal dysplasia 9.9
1838 deafness, autosomal dominant 6/14/38 9.9
1839 blepharospasm, primary benign 9.9
1840 weyers acrofacial dysostosis 9.9
1841 hypouricemia, renal, 2 9.9
1842 muscular dystrophy, limb-girdle, type 1g 9.9
1843 dentin dysplasia, type ii 9.9
1844 adermatoglyphia 9.9
1845 methylmalonic aciduria, vitamin b12-responsive 9.9
1846 bietti crystalline corneoretinal dystrophy 9.9
1847 lung cancer susceptibility 3 9.9
1848 melanoma, cutaneous malignant, 9 9.9
1849 2,4-dienoyl-coa reductase deficiency 9.9
1850 succinyl coa:3-oxoacid coa transferase deficiency 9.9
1851 aplasia of lacrimal and salivary glands 9.9
1852 laron dwarfism 9.9
1853 familial adenomatous polyposis 4 9.9
1854 spinal muscular atrophy-1 9.9
1855 spinal muscular atrophy-3 9.9
1856 sandhoff disease, infantile, juvenile, and adult forms 9.9
1857 mitochondrial complex iii deficiency, nuclear type 8 9.9
1858 deafness, autosomal dominant 1 9.9
1859 clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly 9.9
1860 marinesco-sjogren syndrome 9.9
1861 corneal dystrophy, lattice type i 9.9
1862 corneal dystrophy, avellino type 9.9
1863 carnitine deficiency, systemic primary 9.9
1864 amyotrophic lateral sclerosis 21 9.9
1865 hyperekplexia, hereditary 1, autosomal dominant or recessive 9.9
1866 diastrophic dysplasia 9.9
1867 neuronopathy, distal hereditary motor, type iid 9.9
1868 inflammatory bowel disease 19 9.9
1869 tetralogy of fallot 9.9
1870 frontotemporal dementia and/or amyotrophic lateral sclerosis 3 9.9
1871 immunodeficiency 40 9.9
1872 myeloproliferative/lymphoproliferative neoplasms, familial 9.9
1873 lymphedema, hereditary, ia 9.9
1874 hypoparathyroidism, familial isolated 9.9
1875 leukodystrophy, hypomyelinating, 11 9.9
1876 otospondylomegaepiphyseal dysplasia, autosomal recessive 9.9
1877 adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency 9.9
1878 rahman syndrome 9.9
1879 sarcoidosis 1 9.9
1880 autoinflammation, lipodystrophy, and dermatosis syndrome 9.9
1881 vesicoureteral reflux 8 9.9
1882 wegener granulomatosis 9.9
1883 major depressive disorder and accelerated response to antidepressant drug treatment 9.9
1884 platelet-activating factor acetylhydrolase deficiency 9.9
1885 macular dystrophy, vitelliform, 3 9.9
1886 stickler syndrome, type iv 9.9
1887 arthropathy, progressive pseudorheumatoid, of childhood 9.9
1888 combined oxidative phosphorylation deficiency 11 9.9
1889 coffin-siris syndrome 1 9.9
1890 b-cell expansion with nfkb and t-cell anergy 9.9
1891 baraitser-winter syndrome 1 9.9
1892 crohn disease-associated growth failure 9.9
1893 cold-induced sweating syndrome 3 9.9
1894 pyle disease 9.9
1895 greig cephalopolysyndactyly syndrome 9.9
1896 cerebral cavernous malformations-1 9.9
1897 inflammatory bowel disease 13 9.9
1898 citrullinemia, type ii, neonatal-onset 9.9
1899 hydrops fetalis, nonimmune, and/or atrial septal defect 9.9
1900 osteogenesis imperfecta, type iv 9.9
1901 exudative vitreoretinopathy 5 9.9
1902 inflammatory bowel disease 14 9.9
1903 currarino syndrome 9.9
1904 ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant 9.9
1905 natural killer cell and glucocorticoid deficiency with dna repair defect 9.9
1906 vesicoureteral reflux 3 9.9
1907 mesomelia-synostoses syndrome 9.9
1908 seizures, benign neonatal, type 2 9.9
1909 baller-gerold syndrome 9.9
1910 cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 9.9
1911 nicolaides-baraitser syndrome 9.9
1912 melanoma, cutaneous malignant, 2 9.9
1913 pancreatic cancer/melanoma syndrome 9.9
1914 sialuria 9.9
1915 hyperphosphatasia with mental retardation syndrome 2 9.9
1916 sturge-weber syndrome, somatic, mosaic 9.9
1917 choreoacanthocytosis 9.9
1918 pseudohermaphroditism, male, with gynecomastia 9.9
1919 brachydactyly, type b1 9.9
1920 3-methylglutaconic aciduria, type i 9.9
1921 keratoconus 6 9.9
1922 nail-patella syndrome 9.9
1923 neuropathy, hereditary sensory and autonomic, type viii 9.9
1924 coenzyme q10 deficiency, primary, 7 9.9
1925 epilepsy, nocturnal frontal lobe, 5 9.9
1926 aortic valve disease 1 9.9
1927 renal hypodysplasia/aplasia 1 9.9
1928 cerebrooculofacioskeletal syndrome 1 9.9
1929 nemaline myopathy 11, autosomal recessive 9.9
1930 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 6 9.9
1931 pulmonary fibrosis, idiopathic 9.9
1932 spondyloepiphyseal dysplasia with congenital joint dislocations 9.9
1933 histiocytosis-lymphadenopathy plus syndrome 9.9
1934 leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism 9.9
1935 cowden syndrome 1 9.9
1936 immunodeficiency, common variable, 10 9.9
1937 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 3 9.9
1938 cerebroretinal microangiopathy with calcifications and cysts 2 9.9
1939 combined oxidative phosphorylation deficiency 18 9.9
1940 ceroid lipofuscinosis, neuronal, 10 9.9
1941 thalassemia, hispanic gamma-delta-beta 9.9
1942 fetal hemoglobin quantitative trait locus 1 9.9
1943 neutral lipid storage disease with myopathy 9.9
1944 stormorken syndrome 9.9
1945 hyperinsulinemic hypoglycemia, familial, 1 9.9
1946 epilepsy, progressive myoclonic 7 9.9
1947 potocki-shaffer syndrome 9.9
1948 leukocyte adhesion deficiency, type iii 9.9
1949 encephalopathy, progressive, with or without lipodystrophy 9.9
1950 intrinsic factor deficiency 9.9
1951 multiple endocrine neoplasia 1 9.9
1952 leukemia, acute promyelocytic, somatic 9.9
1953 herpes simplex encephalitis 1 9.9
1954 hypouricemia, renal 9.9
1955 macular dystrophy, vitelliform, 2 9.9
1956 thauvin-robinet-faivre syndrome 9.9
1957 exudative vitreoretinopathy 4 9.9
1958 exudative vitreoretinopathy 1 9.9
1959 combined oxidative phosphorylation deficiency 24 9.9
1960 tremor, hereditary essential, 5 9.9
1961 leukodystrophy, hypomyelinating, 13 9.9
1962 gillessen-kaesbach-nishimura syndrome 9.9
1963 hypoalphalipoproteinemia 9.9
1964 wiedemann-steiner syndrome 9.9
1965 mitochondrial complex ii deficiency 9.9
1966 trehalase deficiency 9.9
1967 inflammatory bowel disease 28, early onset, autosomal recessive 9.9
1968 bleeding disorder, platelet-type, 21 9.9
1969 bartter syndrome, type 2 9.9
1970 hypophosphatemic rickets, autosomal dominant 9.9
1971 keutel syndrome 9.9
1972 megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 9.9
1973 bowen-conradi syndrome 9.9
1974 hemolytic anemia due to triosephosphate isomerase deficiency 9.9
1975 hyperbilirubinemia, rotor type, digenic 9.9
1976 ras-associated autoimmune leukoproliferative disorder 9.9
1977 lamb-shaffer syndrome 9.9
1978 mental retardation, autosomal dominant 6 9.9
1979 epileptic encephalopathy, early infantile, 27 9.9
1980 diarrhea 6 9.9
1981 encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1 9.9
1982 irak4 deficiency 9.9
1983 myoclonus, intractable, neonatal 9.9
1984 meesmann corneal dystrophy 9.9
1985 epidermolysis bullosa simplex, koebner type 9.9
1986 epidermolysis bullosa simplex-mp 9.9
1987 keratosis pilaris atrophicans 9.9
1988 achondrogenesis, type ii or hypochondrogenesis 9.9
1989 smed strudwick type 9.9
1990 czech dysplasia 9.9
1991 kabuki syndrome 1 9.9
1992 melanoma, cutaneous malignant, 3 9.9
1993 corneal dystrophy, congenital stromal 9.9
1994 nephronophthisis 18 9.9
1995 hawkinsinuria 9.9
1996 noonan syndrome 1 9.9
1997 metachondromatosis 9.9
1998 combined oxidative phosphorylation deficiency 31 9.9
1999 spastic ataxia, charlevoix-saguenay type 9.9
2000 muscular dystrophy, limb-girdle, type 2c 9.9
2001 shaheen syndrome 9.9
2002 aicardi-goutieres syndrome 2 9.9
2003 hypotrichosis 8 9.9
2004 neuropathy, hereditary sensory, type id 9.9
2005 lysinuric protein intolerance 9.9
2006 hyperhidrosis palmaris et plantaris 9.9
2007 spastic paraplegia 52, autosomal recessive 9.9
2008 nemaline myopathy 7, autosomal recessive 9.9
2009 microphthalmia with limb anomalies 9.9
2010 methylmalonate semialdehyde dehydrogenase deficiency 9.9
2011 microphthalmia with coloboma 3 9.9
2012 pick disease 9.9
2013 goiter, multinodular 1, with or without sertoli-leydig cell tumors 9.9
2014 mental retardation, autosomal dominant 13 9.9
2015 anemia, sideroblastic, 3, pyridoxine-refractory 9.9
2016 temple syndrome 9.9
2017 corticosteroid-binding globulin deficiency 9.9
2018 cutis laxa, autosomal recessive, type ia 9.9
2019 short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities 9.9
2020 emphysema due to aat deficiency 9.9
2021 pulmonary disease, chronic obstructive 9.9
2022 hydrocephalus, nonsyndromic, autosomal recessive 9.9
2023 melanoma, cutaneous malignant, 6 9.9
2024 mosaic variegated aneuploidy syndrome 1 9.9
2025 bartter syndrome, type 1 9.9
2026 peeling skin syndrome 2 9.9
2027 stiff skin syndrome 9.9
2028 lethal congenital contracture syndrome 11 9.9
2029 hepatic lipase deficiency 9.9
2030 tay-sachs disease 9.9
2031 tyrosinemia, type i 9.9
2032 acrocallosal syndrome 9.9
2033 bloom syndrome 9.9
2034 spinocerebellar ataxia, autosomal recessive 16 9.9
2035 beaulieu-boycott-innes syndrome 9.9
2036 familial adenomatous polyposis 3 9.9
2037 pseudoxanthoma elasticum 9.9
2038 microhydranencephaly 9.9
2039 familial mediterranean fever, ar 9.9
2040 glycogen storage disease ixc 9.9
2041 tremor, hereditary essential, 4 9.9
2042 generalized epilepsy with febrile seizures plus, type 9 9.9
2043 blau syndrome 9.9
2044 spinocerebellar ataxia, autosomal recessive 12 9.9
2045 kbg syndrome 9.9
2046 mucopolysaccharidosis iva 9.9
2047 uv-induced skin damage 9.9
2048 melanoma, cutaneous malignant, 5 9.9
2049 pontocerebellar hypoplasia, type 2e 9.9
2050 li-fraumeni syndrome 9.9
2051 myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiency 9.9
2052 mitochondrial complex iii deficiency, nuclear type 2 9.9
2053 immunoglobulin a deficiency 2 9.9
2054 combined oxidative phosphorylation deficiency 17 9.9
2055 renal cysts and diabetes syndrome 9.9
2056 pachyonychia congenita 1 9.9
2057 epilepsy, progressive myoclonic 6 9.9
2058 hyper-ige recurrent infection syndrome 9.9
2059 mandibulofacial dysostosis, guion-almeida type 9.9
2060 frontotemporal lobar degeneration with ubiquitin-positive inclusions 9.9
2061 ceroid lipofuscinosis, neuronal, 11 9.9
2062 bleeding disorder, platelet-type, 16, autosomal dominant 9.9
2063 mulibrey nanism 9.9
2064 specific granule deficiency 2 9.9
2065 paramyotonia congenita 9.9
2066 sessile serrated polyposis cancer syndrome 9.9
2067 sarcoma, synovial 9.9
2068 hypotrichosis 6 9.9
2069 tenorio syndrome 9.9
2070 left ventricular noncompaction 1, with or without congenital heart defects 9.9
2071 cholestasis, progressive familial intrahepatic 1 9.9
2072 cholestasis, benign recurrent intrahepatic 9.9
2073 pitt-hopkins syndrome 9.9
2074 neutropenia, cyclic 9.9
2075 boucher-neuhauser syndrome 9.9
2076 oliver-mcfarlane syndrome 9.9
2077 spondyloenchondrodysplasia with immune dysregulation 9.9
2078 coffin-siris syndrome 4 9.9
2079 aicardi-goutieres syndrome 4 9.9
2080 amelogenesis imperfecta, type ij 9.9
2081 efavirenz, poor metabolism of 9.9
2082 3-m syndrome 3 9.9
2083 megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 9.9
2084 ciliary dyskinesia, primary, 20 9.9
2085 bleeding disorder, platelet-type, 11 9.9
2086 polyglucosan body myopathy 1 with or without immunodeficiency 9.9
2087 fazio-londe disease 9.9
2088 epileptic encephalopathy, early infantile, 12 9.9
2089 aicardi-goutieres syndrome 5 9.9
2090 multicentric carpotarsal osteolysis syndrome 9.9
2091 thrombocytopenia 6 9.9
2092 inflammatory bowel disease 25, early onset, autosomal recessive 9.9
2093 holocarboxylase synthetase deficiency 9.9
2094 parkinson disease 20, early-onset 9.9
2095 coffin-siris syndrome 3 9.9
2096 adenylosuccinase deficiency 9.9
2097 infantile cerebellar-retinal degeneration 9.9
2098 pigmentary disorder, reticulate, with systemic manifestations, x-linked 9.9
2099 hypophosphatemic rickets, x-linked dominant 9.9
2100 epileptic encephalopathy, early infantile, 1 9.9
2101 aicardi syndrome 9.9
2102 exudative vitreoretinopathy 2, x-linked 9.9
2103 chondrodysplasia punctata, x-linked dominant 9.9
2104 wieacker-wolff syndrome 9.9
2105 megalocornea 1, x-linked 9.9
2106 epileptic encephalopathy, early infantile, 36 9.9
2107 tn polyagglutination syndrome, somatic 9.9
2108 xq25 duplication syndrome 9.9
2109 lymphoproliferative syndrome, x-linked, 1 9.9
2110 vacterl association, x-linked 9.9
2111 myopathy, x-linked, with postural muscle atrophy 9.9
2112 immunodeficiency 47 9.9
2113 dyskeratosis congenita, x-linked 9.9
2114 mental retardation, x-linked syndromic, lubs type 9.9
2115 autism x-linked 6 9.9
2116 myopathy, x-linked, with excessive autophagy 9.9
2117 roussy-levy syndrome 9.9
2118 escobar syndrome 9.9
2119 fuhrmann syndrome 9.9
2120 meleda disease 9.9
2121 hyperinsulinism-hyperammonemia syndrome 9.9
2122 image syndrome 9.9
2123 centrotemporal epilepsy 9.9
2124 progressive external ophthalmoplegia, autosomal dominant 1 9.9
2125 vlcad deficiency 9.9
2126 van buchem disease 9.9
2127 hyperferritinemia-cataract syndrome 9.9
2128 partington syndrome 9.9
2129 child syndrome 9.9
2130 neuropathy, ataxia, and retinitis pigmentosa 9.9
2131 ermine phenotype 9.9
2132 blue rubber bleb nevus 9.9
2133 hemochromatosis, neonatal 9.9
2134 lymphangiectasia, pulmonary, congenital 9.9
2135 laryngomalacia 9.9
2136 scheuermann disease 9.9
2137 goodpasture syndrome 9.9
2138 jejunal atresia 9.9
2139 paget disease, extramammary 9.9
2140 lipomatosis, multiple 9.9
2141 gastritis, familial giant hypertrophic 9.9
2142 blepharochalasis and double lip 9.9
2143 cheilitis glandularis 9.9
2144 chromosome 2q35 duplication syndrome 9.9
2145 pacman dysplasia 9.9
2146 hypertrichosis, congenital generalized, with or without gingival hyperplasia 9.9
2147 otodental dysplasia 9.9
2148 pyknoachondrogenesis 9.9
2149 pontine tegmental cap dysplasia 9.9
2150 pentosuria 9.9
2151 hemangiopericytoma, malignant 9.9
2152 intracranial hypertension, idiopathic 9.9
2153 respiratory distress syndrome in premature infants 9.9
2154 amyotrophy, monomelic 9.9
2155 heart block, congenital 9.9
2156 nail disorder, nonsyndromic congenital, 1 9.9
2157 hyperostosis frontalis interna 9.9
2158 lipedema 9.9
2159 felty syndrome 9.9
2160 interstitial pneumonitis, desquamative, familial 9.9
2161 acute lymphoblastic leukemia, childhood 9.9
2162 intraocular lymphoma 9.9
2163 kartagener syndrome 9.9
2164 temporomandibular ankylosis 9.9
2165 foodborne botulism 9.9
2166 carrion's disease 9.9
2167 familial partial lipodystrophy 9.9
2168 2-hydroxyglutaric aciduria 9.9
2169 hereditary lymphedema 9.9
2170 opitz-gbbb syndrome 9.9
2171 villous adenoma 9.9
2172 pervasive developmental disorder 9.9
2173 benign familial infantile epilepsy 9.9
2174 agraphia 9.9
2175 acrofrontofacionasal dysostosis 9.9
2176 primary pigmented nodular adrenocortical disease 9.9
2177 inguinal hernia 9.9
2178 autosomal dominant nocturnal frontal lobe epilepsy 9.9
2179 acromesomelic dysplasia 9.9
2180 congenital fiber-type disproportion 9.9
2181 bladder exstrophy-epispadias-cloacal exstrophy complex 9.9
2182 neurodegeneration with brain iron accumulation 9.9
2183 hemochromatosis type 2 9.9
2184 nodular malignant melanoma 9.9
2185 dry eye syndrome 9.9
2186 cholelithiasis 9.9
2187 exhibitionism 9.9
2188 steatorrhea 9.9
2189 dirofilariasis 9.9
2190 eastern equine encephalitis 9.9
2191 salivary gland disease 9.9
2192 obsessive-compulsive personality disorder 9.9
2193 paranoid personality disorder 9.9
2194 cholecystolithiasis 9.9
2195 cercarial dermatitis 9.9
2196 expressive language disorder 9.9
2197 polydactyly 9.9
2198 fissured tongue 9.9
2199 cauda equina syndrome 9.9
2200 prediabetes syndrome 9.9
2201 kohler's disease 9.9
2202 pulmonary hemosiderosis 9.9
2203 filarial elephantiasis 9.9
2204 vogt-koyanagi-harada disease 9.9
2205 idiopathic juvenile osteoporosis 9.9
2206 vestibular neuronitis 9.9
2207 mixed receptive-expressive language disorder 9.9
2208 intermediate uveitis 9.9
2209 miller fisher syndrome 9.9
2210 allergic bronchopulmonary aspergillosis 9.9
2211 congenital dyserythropoietic anemia 9.9
2212 color blindness 9.9
2213 acute gonococcal cystitis 9.9
2214 beriberi 9.9
2215 fox-fordyce disease 9.9
2216 necrotizing ulcerative gingivitis 9.9
2217 geniculate ganglionitis 9.9
2218 ureteral disease 9.9
2219 primary hypertrophic osteoarthropathy 9.9
2220 critical illness polyneuropathy 9.9
2221 cholesterol ester storage disease 9.9
2222 reye syndrome 9.9
2223 papilledema 9.9
2224 labyrinthitis 9.9
2225 branchiootorenal syndrome 9.9
2226 benign familial neonatal epilepsy 9.9
2227 nodular nonsuppurative panniculitis 9.9
2228 pleural disease 9.9
2229 sphingolipidosis 9.9
2230 hypothalamic disease 9.9
2231 trichomoniasis 9.9
2232 carbuncle 9.9
2233 infantile epileptic encephalopathy 9.9