BMIQ12
MCID: BDY015
MIFTS: 46

Body Mass Index Quantitative Trait Locus 12 (BMIQ12)

Categories: Bone diseases, Genetic diseases, Metabolic diseases

Aliases & Classifications for Body Mass Index Quantitative Trait Locus 12

MalaCards integrated aliases for Body Mass Index Quantitative Trait Locus 12:

Name: Body Mass Index Quantitative Trait Locus 12 56 29 6 39
Obesity, Susceptibility to, Bmiq12 56 13
Obesity 56 71
Obesity, Susceptibility to 56
Obesity Bmiq12 56
Bmiq12 56

Classifications:



External Ids:

OMIM 56 612362
UMLS 71 C0028754

Summaries for Body Mass Index Quantitative Trait Locus 12

MalaCards based summary : Body Mass Index Quantitative Trait Locus 12, also known as obesity, susceptibility to, bmiq12, is related to syndromic obesity and proprotein convertase 1/3 deficiency, and has symptoms including symptoms, high weight and obesity, metabolically benign. An important gene associated with Body Mass Index Quantitative Trait Locus 12 is PCSK1 (Proprotein Convertase Subtilisin/Kexin Type 1). The drugs Citalopram and Oseltamivir have been mentioned in the context of this disorder. Affiliated tissues include liver, heart and breast.

More information from OMIM: 612362

Related Diseases for Body Mass Index Quantitative Trait Locus 12

Diseases in the Body Mass Index Quantitative Trait Locus 11 family:

Body Mass Index Quantitative Trait Locus 9 Body Mass Index Quantitative Trait Locus 8
Body Mass Index Quantitative Trait Locus 1 Body Mass Index Quantitative Trait Locus 2
Body Mass Index Quantitative Trait Locus 3 Body Mass Index Quantitative Trait Locus 4
Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 7
Body Mass Index Quantitative Trait Locus 5 Body Mass Index Quantitative Trait Locus 6
Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 13
Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 15
Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 19
Body Mass Index Quantitative Trait Locus 20

Diseases related to Body Mass Index Quantitative Trait Locus 12 via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 2055, show less)
# Related Disease Score Top Affiliating Genes
1 syndromic obesity 32.4 PCSK1 LOC101929710
2 proprotein convertase 1/3 deficiency 32.2 PCSK1 LOC101929710
3 body mass index quantitative trait locus 11 12.7
4 obesity, early-onset, with adrenal insufficiency and red hair 12.7
5 morbid obesity and spermatogenic failure 12.7
6 leptin deficiency or dysfunction 12.6
7 obesity-hypoventilation syndrome 12.6
8 genetic obesity 12.6
9 abdominal obesity-metabolic syndrome quantitative trait locus 2 12.6
10 mental retardation, truncal obesity, retinal dystrophy, and micropenis syndrome 12.5
11 obesity, hyperphagia, and developmental delay 12.5
12 abdominal obesity-metabolic syndrome 1 12.5
13 spastic paraplegia, intellectual disability, nystagmus, and obesity 12.5
14 retinal dystrophy and obesity 12.5
15 wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome 12.5
16 abdominal obesity-metabolic syndrome 3 12.5
17 hypothalamic obesity 12.5
18 hydrocephalus obesity hypogonadism 12.5
19 x-linked intellectual disability - short stature - obesity 12.4
20 abdominal obesity-metabolic syndrome 4 12.4
21 body mass index quantitative trait locus 19 12.4
22 leptin receptor deficiency 12.4
23 body mass index quantitative trait locus 20 12.3
24 aniridia - ptosis - intellectual disability - familial obesity 12.3
25 obesity due to melanocortin 4 receptor deficiency 12.3
26 rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome 12.3
27 coloboma-obesity-hypogenitalism-mental retardation syndrome 12.3
28 obesity due to sim1 deficiency 12.3
29 short stature-obesity syndrome 12.2
30 mental retardation, obesity, mandibular prognathism, and eye and skin anomalies 12.2
31 prolactin deficiency with obesity and enlarged testes 12.2
32 cohen syndrome 12.2
33 obesity due to congenital leptin resistance 12.2
34 severe early-onset obesity-insulin resistance syndrome due to sh2b1 deficiency 12.2
35 wilson-turner x-linked mental retardation syndrome 12.2
36 body mass index quantitative trait locus 9 12.2
37 body mass index quantitative trait locus 4 12.2
38 midface hypoplasia, obesity, developmental delay, and neonatal hypotonia 12.2
39 body mass index quantitative trait locus 14 12.2
40 body mass index quantitative trait locus 8 12.2
41 body mass index quantitative trait locus 7 12.2
42 body mass index quantitative trait locus 18 12.2
43 mehmo syndrome 12.2
44 body mass index quantitative trait locus 10 12.1
45 genetic non-syndromic obesity 12.1
46 momo syndrome 12.1
47 chung-jansen syndrome 12.1
48 chops syndrome 12.1
49 genetic overgrowth/obesity syndrome 12.0
50 overgrowth/obesity syndrome 12.0
51 x-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome 12.0
52 intellectual disability-seizures-macrocephaly-obesity syndrome 12.0
53 intellectual disability-obesity-brain malformations-facial dysmorphism syndrome 12.0
54 obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome 12.0
55 ayazi syndrome 11.9
56 rohhad 11.9
57 coenzyme q10 deficiency, primary, 2 11.8
58 hyperostosis frontalis interna 11.8
59 fatty liver disease 11.7
60 polycystic ovary syndrome 11.7
61 prader-willi syndrome 11.7
62 man1b1-cdg 11.7
63 non-alcoholic fatty liver disease 11.7
64 diabetes mellitus, noninsulin-dependent 11.7
65 alstrom syndrome 11.6
66 bardet-biedl syndrome 11.6
67 carpenter syndrome 1 11.6
68 glucose intolerance 11.6
69 eating disorder 11.6
70 sleep apnea 11.6
71 bardet-biedl syndrome 1 11.6
72 pseudohypoparathyroidism, type ia 11.6
73 borjeson-forssman-lehmann syndrome 11.6
74 fatty liver disease, nonalcoholic 1 11.5
75 chromosome 16p11.2 deletion syndrome, 220-kb 11.5
76 bardet-biedl syndrome 3 11.5
77 mental retardation, autosomal dominant 39 11.5
78 gestational diabetes 11.5
79 conn's syndrome 11.5
80 hypertriglyceridemia, familial 11.5
81 prediabetes syndrome 11.5
82 gallbladder disease 1 11.5
83 bardet-biedl syndrome 4 11.5
84 non-alcoholic steatohepatitis 11.5
85 bardet-biedl syndrome 2 11.5
86 laron syndrome 11.5
87 pseudopseudohypoparathyroidism 11.5
88 pre-eclampsia 11.4
89 rickets 11.4
90 vascular disease 11.4
91 diabetes mellitus, ketosis-prone 11.4
92 bardet-biedl syndrome 6 11.4
93 pituitary adenoma 4, acth-secreting 11.4
94 wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 11.4
95 achondroplasia 11.4
96 acanthosis nigricans 11.4
97 bardet-biedl syndrome 9 11.4
98 adiposis dolorosa 11.4
99 bardet-biedl syndrome 5 11.4
100 hyperlipoproteinemia, type iii 11.4
101 bardet-biedl syndrome 7 11.4
102 breast cancer 11.4
103 pulmonary embolism 11.4
104 aromatase deficiency 11.4
105 bardet-biedl syndrome 8 11.4
106 bardet-biedl syndrome 10 11.4
107 bardet-biedl syndrome 14 11.4
108 bardet-biedl syndrome 21 11.4
109 kleefstra syndrome 11.4
110 camera-marugo-cohen syndrome 11.4
111 clark-baraitser syndrome 11.4
112 biemond syndrome ii 11.4
113 hepatocellular carcinoma 11.3
114 hernia, hiatus 11.3
115 migraine with or without aura 1 11.3
116 gout 11.3
117 neural tube defects 11.3
118 renal cell carcinoma, nonpapillary 11.3
119 focal segmental glomerulosclerosis 11.3
120 stroke, ischemic 11.3
121 varicose veins 11.3
122 esophageal cancer 11.3
123 myeloma, multiple 11.3
124 hidradenitis suppurativa 11.3
125 mckusick-kaufman syndrome 11.3
126 hypersomnia 11.3
127 adiponectin, serum level of, quantitative trait locus 1 11.3
128 body mass index quantitative trait locus 1 11.3
129 blount's disease 11.3
130 acth-secreting pituitary adenoma 11.3
131 smith-magenis syndrome 11.2
132 empty sella syndrome 11.2
133 monogenic diabetes 11.2
134 alopecia, androgenetic, 1 11.2
135 polycystic ovary syndrome 1 11.2
136 chromosome 16p13.3 deletion syndrome, proximal 11.2
137 schaaf-yang syndrome 11.2
138 idiopathic edema 11.2
139 primary pigmented nodular adrenocortical disease 11.2
140 bell's palsy 11.2
141 hyperadrenalism 11.2
142 maturity-onset diabetes of the young, type 2 11.2
143 mental retardation, x-linked, syndromic, cabezas type 11.2
144 microvascular complications of diabetes 1 11.2
145 neutral lipid storage disease with myopathy 11.2
146 syndromic x-linked intellectual disability 7 11.2
147 carcinosarcoma 11.2
148 froelich syndrome 11.2
149 classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 11.2
150 bardet-biedl syndrome 12 11.2
151 ulnar-mammary syndrome 11.1
152 pseudohypoparathyroidism, type ic 11.1
153 lipid metabolism disorder 11.1
154 hyperinsulinism 11.1
155 acrodysostosis 1 with or without hormone resistance 11.1
156 chromosome 16p12.1 deletion syndrome, 520-kb 11.1
157 growth hormone insensitivity with immunodeficiency 11.1
158 prader-willi habitus, osteopenia, and camptodactyly 11.1
159 chromosome 2q37 deletion syndrome 11.1
160 chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb 11.1
161 carpenter syndrome 2 11.1
162 pigmented nodular adrenocortical disease, primary, 4 11.1
163 bardet-biedl syndrome 11 11.1
164 bardet-biedl syndrome 13 11.1
165 bardet-biedl syndrome 16 11.1
166 bardet-biedl syndrome 17 11.1
167 bardet-biedl syndrome 18 11.1
168 bardet-biedl syndrome 19 11.1
169 bardet-biedl syndrome 20 11.1
170 intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures 11.1
171 cortisone reductase deficiency 11.1
172 pelvic lipomatosis 11.1
173 short stature, brachydactyly, intellectual developmental disability, and seizures 11.0
174 liver disease 11.0
175 hyperglycemia 11.0
176 diabetes mellitus 10.9
177 pituitary adenoma 1, multiple types 10.9
178 cockayne syndrome b 10.9
179 hepatitis b vaccine, response to 10.9
180 precocious puberty, central, 1 10.9
181 septooptic dysplasia 10.9
182 cerebrooculofacioskeletal syndrome 1 10.9
183 acth-independent macronodular adrenal hyperplasia 10.9
184 mental retardation, x-linked, syndromic, nascimento type 10.9
185 chromosome xq27.3-q28 duplication syndrome 10.9
186 diabetes mellitus, noninsulin-dependent, 1 10.9
187 renal cell carcinoma, papillary, 1 10.9
188 high density lipoprotein cholesterol level quantitative trait locus 1 10.9
189 coronary artery disease, autosomal dominant, 1 10.9
190 lipodystrophy, familial partial, type 1 10.9
191 pigmented nodular adrenocortical disease, primary, 2 10.9
192 pigmented nodular adrenocortical disease, primary, 1 10.9
193 diabetes mellitus, insulin-resistant, with acanthosis nigricans 10.9
194 chromosome 3q29 duplication syndrome 10.9
195 pigmented nodular adrenocortical disease, primary, 3 10.9
196 precocious puberty, central, 2 10.9
197 helsmoortel-van der aa syndrome 10.9
198 acth-independent macronodular adrenal hyperplasia 2 10.9
199 bardet-biedl syndrome 15 10.9
200 diabetes mellitus, noninsulin-dependent, 5 10.9
201 temple syndrome 10.9
202 white-sutton syndrome 10.9
203 senior-loken syndrome 9 10.9
204 luscan-lumish syndrome 10.9
205 chromosome 15q24 deletion syndrome 10.9
206 chromosome 16p11.2 deletion syndrome 10.9
207 syndromic x-linked intellectual disability shashi type 10.9
208 48,xxyy syndrome 10.9
209 cerebro-oculo-facio-skeletal syndrome 10.9
210 hernández-aguirre negrete syndrome 10.9
211 lipodermatosclerosis 10.9
212 localized lipodystrophy 10.9
213 macular telangiectasia type 2 10.9
214 male pseudohermaphroditism intellectual disability syndrome, verloes type 10.9
215 mthfr gene variant 10.9
216 proximal chromosome 18q deletion syndrome 10.9
217 coronary heart disease 1 10.8
218 hypercholesterolemia, familial, 1 10.8
219 gastroesophageal reflux 10.8
220 osteoarthritis 10.7
221 heart disease 10.7
222 chronic kidney disease 10.7
223 atherosclerosis susceptibility 10.7
224 kidney disease 10.7
225 endometrial cancer 10.7
226 hypoglycemia 10.7
227 asthma 10.7
228 congestive heart failure 10.7
229 hypogonadism 10.7
230 lipedema 10.6
231 apnea, obstructive sleep 10.6
232 hyperandrogenism 10.6
233 overnutrition 10.6
234 hypertension, essential 10.6
235 colorectal cancer 10.6
236 hypothyroidism 10.6
237 infertility 10.6
238 depression 10.6
239 anorexia nervosa 10.6
240 hyperuricemia 10.6
241 periodontitis 10.6
242 end stage renal disease 10.6
243 lipoprotein quantitative trait locus 10.6
244 hypervitaminosis d 10.6
245 arteries, anomalies of 10.6
246 respiratory failure 10.6
247 insulin-like growth factor i 10.6
248 placenta disease 10.6
249 sleep disorder 10.5
250 autoimmune disease 10.5
251 anxiety 10.5
252 rapidly involuting congenital hemangioma 10.5
253 atrial fibrillation 10.5
254 impotence 10.5
255 attention deficit-hyperactivity disorder 10.5
256 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.5
257 pustulosis of palm and sole 10.5
258 psoriasis 10.5
259 proteasome-associated autoinflammatory syndrome 1 10.5
260 esophagitis 10.5
261 thyroiditis 10.5
262 hair whorl 10.5
263 eclampsia 10.5
264 osteoporosis 10.5
265 cytokine deficiency 10.5
266 bone mineral density quantitative trait locus 8 10.5
267 bone mineral density quantitative trait locus 15 10.5
268 iron metabolism disease 10.5
269 mood disorder 10.5
270 microvascular complications of diabetes 3 10.5
271 microvascular complications of diabetes 4 10.5
272 microvascular complications of diabetes 6 10.5
273 microvascular complications of diabetes 7 10.5
274 mental depression 10.5
275 dental caries 10.5
276 liver cirrhosis 10.5
277 prostate cancer 10.5
278 bulimia nervosa 10.5
279 major depressive disorder 10.5
280 aging 10.5
281 overgrowth syndrome 10.5
282 cholelithiasis 10.4
283 nephrolithiasis 10.4
284 alacrima, achalasia, and mental retardation syndrome 10.4
285 cardiovascular system disease 10.4
286 diabetes mellitus, type i 10.4
287 acute pancreatitis 10.4
288 back pain 10.4
289 pancreatic cancer 10.4
290 pulmonary hypertension 10.4
291 severe combined immunodeficiency 10.4
292 resting heart rate, variation in 10.4
293 anovulation 10.4
294 adenoma 10.4
295 47,xyy 10.4
296 constipation 10.4
297 thrombophilia due to thrombin defect 10.4
298 hypoxia 10.4
299 hashimoto thyroiditis 10.4
300 acute insulin response 10.4
301 neuropathy 10.4
302 inflammatory bowel disease 10.4
303 hyperparathyroidism 10.4
304 myocardial infarction 10.4
305 48,xyyy 10.4
306 atrial standstill 1 10.4
307 gallbladder disease 10.4
308 bipolar disorder 10.4
309 covid-19 10.4
310 major affective disorder 8 10.4
311 major affective disorder 9 10.4
312 adenocarcinoma 10.4
313 kidney cancer 10.4
314 pulmonary disease, chronic obstructive 10.4
315 arteriosclerosis 10.4
316 bone resorption disease 10.4
317 barrett esophagus 10.4
318 ischemia 10.4
319 cerebrovascular disease 10.4
320 peripheral vascular disease 10.4
321 craniopharyngioma 10.4
322 autonomic dysfunction 10.4
323 sexual disorder 10.4
324 chronic pain 10.4
325 lung disease 10.4
326 fetal macrosomia 10.4
327 alcohol dependence 10.4
328 intracranial hypertension 10.4
329 hereditary lymphedema i 10.4
330 diarrhea 10.4
331 huntington disease-like 2 10.4
332 pain agnosia 10.4
333 ige responsiveness, atopic 10.4
334 leukemia, acute lymphoblastic 10.4
335 autism spectrum disorder 10.4
336 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.3
337 rectum cancer 10.3
338 alzheimer disease 10.3
339 pancreatitis 10.3
340 down syndrome 10.3
341 alcohol use disorder 10.3
342 dysphagia 10.3
343 headache 10.3
344 disease of mental health 10.3
345 gastritis 10.3
346 nutritional deficiency disease 10.3
347 autism 10.3
348 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 10.3
349 periodontitis, chronic 10.3
350 secondary hyperparathyroidism 10.3
351 cardiac conduction defect 10.3
352 microvascular complications of diabetes 5 10.3
353 male infertility 10.3
354 fibrosis of extraocular muscles, congenital, 1 10.3
355 hypogonadotropic hypogonadism 10.3
356 rhinitis 10.3
357 peripheral nervous system disease 10.3
358 thrombosis 10.3
359 cholecystitis 10.3
360 acute myocardial infarction 10.3
361 amenorrhea 10.3
362 thyroid carcinoma 10.3
363 personality disorder 10.3
364 prostatic hypertrophy 10.3
365 acute cystitis 10.3
366 appendicitis 10.3
367 rheumatoid arthritis 10.3
368 hypotonia 10.3
369 urolithiasis 10.3
370 substance abuse 10.3
371 spinal cord injury 10.3
372 ovarian cancer 10.3
373 allergic rhinitis 10.3
374 neurofibromatosis, type ii 10.3
375 prostatic adenoma 10.3
376 prostatic hyperplasia, benign 10.3
377 gastric cancer 10.3
378 dementia 10.3
379 acute kidney failure 10.3
380 pik3ca-related overgrowth syndrome 10.3
381 allergic asthma 10.3
382 deficiency anemia 10.3
383 colorectal adenoma 10.3
384 ovarian disease 10.3
385 toxic shock syndrome 10.3
386 muscular atrophy 10.3
387 intracranial hypertension, idiopathic 10.2
388 dermatitis, atopic 10.2
389 alexithymia 10.2
390 skin disease 10.2
391 nephrolithiasis, calcium oxalate 10.2
392 psoriatic arthritis 10.2
393 schizophrenia 10.2
394 huntington disease-like 3 10.2
395 peptic esophagitis 10.2
396 insulinoma 10.2
397 crohn's disease 10.2
398 hypopituitarism 10.2
399 growth hormone deficiency 10.2
400 cardiac arrest 10.2
401 bone disease 10.2
402 influenza 10.2
403 arthritis 10.2
404 lipomatosis 10.2
405 fibromyalgia 10.2
406 cellulitis 10.2
407 peritonitis 10.2
408 pelvic organ prolapse 10.2
409 venous insufficiency 10.2
410 dumping syndrome 10.2
411 precocious puberty 10.2
412 hypervitaminosis a 10.2
413 carotenemia 10.2
414 helicobacter pylori infection 10.2
415 yemenite deaf-blind hypopigmentation syndrome 10.2
416 viral hepatitis 10.2
417 hyperthyroidism 10.2
418 encephalopathy 10.2
419 celiac disease 1 10.2
420 low compliance bladder 10.2
421 avoidant personality disorder 10.2
422 dermatitis 10.2
423 ileus 10.2
424 irritable bowel syndrome 10.2
425 colitis 10.2
426 aortic aneurysm 10.2
427 homocysteinemia 10.2
428 leukemia, acute lymphoblastic 3 10.2
429 angina pectoris 10.2
430 autonomic neuropathy 10.2
431 nephrotic syndrome 10.2
432 hepatitis c 10.2
433 arthropathy 10.2
434 peptic ulcer disease 10.2
435 ulcerative colitis 10.2
436 triiodothyronine receptor auxiliary protein 10.2
437 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 10.2
438 hyperprolactinemia 10.2
439 diverticulitis 10.2
440 aortic aneurysm, familial abdominal, 1 10.2
441 multiple sclerosis 10.2
442 cervical cancer 10.2
443 muscle hypertrophy 10.2
444 endometrial hyperplasia 10.2
445 cerebral palsy 10.2
446 bladder cancer 10.2
447 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 10.2
448 gastrojejunal ulcer 10.2
449 hemosiderosis 10.2
450 gingivitis 10.2
451 aneurysm 10.2
452 polyneuropathy 10.1
453 severe acute respiratory syndrome 10.1
454 schizoaffective disorder 10.1
455 pneumonia 10.1
456 bronchitis 10.1
457 b-cell lymphoma 10.1
458 intussusception 10.1
459 lung cancer 10.1
460 anemia, x-linked, with or without neutropenia and/or platelet abnormalities 10.1
461 wernicke encephalopathy 10.1
462 cataract 10.1
463 learning disability 10.1
464 narcolepsy 10.1
465 postpartum depression 10.1
466 systolic heart failure 10.1
467 systemic lupus erythematosus 10.1
468 renal fibrosis 10.1
469 iron deficiency anemia 10.1
470 goiter 10.1
471 pulmonary hypertension, primary, 1 10.1
472 metabolic acidosis 10.1
473 gastric ulcer 10.1
474 pulmonary edema 10.1
475 allergic hypersensitivity disease 10.1
476 dilated cardiomyopathy 10.1
477 keratosis 10.1
478 heart valve disease 10.1
479 achalasia 10.1
480 rare hereditary hemochromatosis 10.1
481 ciliopathy 10.1
482 lymphoma, hodgkin, classic 10.1
483 hypogonadism, male 10.1
484 ectodermal dysplasia-syndactyly syndrome 2 10.1
485 lupus erythematosus 10.1
486 slipped capital femoral epiphysis 10.1
487 polydactyly 10.1
488 creatinine clearance quantitative trait locus 10.1
489 limb ischemia 10.1
490 lymphoma 10.1
491 endometritis 10.1
492 neutropenia 10.1
493 paraplegia 10.1
494 ovarian epithelial cancer 10.1
495 lymphoma, non-hodgkin, familial 10.1
496 bone mineral density quantitative trait locus 3 10.1
497 vitamin b12 deficiency 10.1
498 scoliosis 10.1
499 childhood acute lymphocytic leukemia 10.1
500 hydrocephalus 10.1
501 familial hyperlipidemia 10.1
502 leukemia 10.1
503 hepatitis b 10.1
504 coronary stenosis 10.1
505 compartment syndrome 10.1
506 polycythemia 10.1
507 intermediate coronary syndrome 10.1
508 dwarfism 10.1
509 leukemia, acute myeloid 10.1
510 chorioamnionitis 10.1
511 pancreatic ductal adenocarcinoma 10.1
512 lactic acidosis 10.1
513 pseudohypoparathyroidism 10.1
514 intestinal obstruction 10.1
515 hypereosinophilic syndrome 10.1
516 cryptogenic cirrhosis 10.1
517 carpal tunnel syndrome 10.1
518 otitis media 10.1
519 ataxia and polyneuropathy, adult-onset 10.1
520 maturity-onset diabetes of the young 10.1
521 helix syndrome 10.1
522 autosomal recessive disease 10.1
523 physical disorder 10.1
524 sialadenitis 10.1
525 infant gynecomastia 10.1
526 hypertrophic cardiomyopathy 10.1
527 gynecomastia 10.1
528 myeloid leukemia 10.1
529 diabetes insipidus 10.1
530 alopecia 10.1
531 premature aging 10.1
532 tobacco addiction 10.1
533 arts syndrome 10.1
534 bacterial infectious disease 10.1
535 hypertensive heart disease 10.1
536 plica syndrome 10.1
537 beriberi 10.1
538 duodenal ulcer 10.1
539 post-traumatic stress disorder 10.1
540 synovitis 10.1
541 acute stress disorder 10.1
542 spinal stenosis 10.1
543 situs inversus 10.1
544 meningioma, radiation-induced 10.0
545 meningioma, familial 10.0
546 smoking as a quantitative trait locus 3 10.0
547 melanoma, cutaneous malignant 10 10.0
548 gastrointestinal ulceration, recurrent, with dysfunctional platelets 10.0
549 peripheral artery disease 10.0
550 chronic venous insufficiency 10.0
551 spinal meningioma 10.0
552 melanoma 10.0
553 hidradenitis 10.0
554 iga glomerulonephritis 10.0
555 hypokalemia 10.0
556 secretory meningioma 10.0
557 lymphoplasmacyte-rich meningioma 10.0
558 retinal degeneration 10.0
559 brain injury 10.0
560 obsessive-compulsive disorder 10.0
561 hutterite cerebroosteonephrodysplasia syndrome 10.0
562 ocular motor apraxia 10.0
563 macular degeneration, age-related, 1 10.0
564 gastrointestinal stromal tumor 10.0
565 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.0
566 diffuse large b-cell lymphoma 10.0
567 diphtheria 10.0
568 thrombocytopenia 10.0
569 enthesopathy 10.0
570 acromegaly 10.0
571 endometriosis 10.0
572 gallbladder cancer 10.0
573 skin carcinoma 10.0
574 bladder disease 10.0
575 glucose metabolism disease 10.0
576 clear cell renal cell carcinoma 10.0
577 panic disorder 10.0
578 gastrointestinal system disease 10.0
579 vascular dementia 10.0
580 fasciitis 10.0
581 diastolic heart failure 10.0
582 simpson-golabi-behmel syndrome 10.0
583 hypercarotenemia and vitamin a deficiency, autosomal dominant 10.0
584 spondylolisthesis 10.0
585 osteomalacia 10.0
586 keratomalacia 10.0
587 gastroparesis 10.0
588 conduct disorder 10.0
589 cholestasis 10.0
590 familial hypercholesterolemia 10.0
591 thrombophilia 10.0
592 psychotic disorder 10.0
593 bilirubin metabolic disorder 10.0
594 intermittent claudication 10.0
595 pancreatic adenocarcinoma 10.0
596 pituitary gland disease 10.0
597 degenerative disc disease 10.0
598 diabetic neuropathy 10.0
599 drug dependence 10.0
600 allergic encephalomyelitis 10.0
601 dentinogenesis imperfecta type 2 10.0
602 seizure disorder 10.0
603 traumatic brain injury 10.0
604 hyperlipidemia, familial combined, 3 10.0
605 optic atrophy 1 10.0
606 cryptorchidism, unilateral or bilateral 10.0
607 cystic fibrosis 10.0
608 retinitis pigmentosa 10.0
609 mend syndrome 10.0
610 taqi polymorphism 10.0
611 global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 10.0
612 pyelonephritis 10.0
613 acute leukemia 10.0
614 candidiasis 10.0
615 retinal vascular disease 10.0
616 pancreas disease 10.0
617 thyroid gland disease 10.0
618 chromosomal triplication 10.0
619 dextrocardia with situs inversus 10.0
620 paresthesia 10.0
621 glomerular disease 10.0
622 retinoblastoma 10.0
623 graft-versus-host disease 10.0
624 fetal akinesia deformation sequence 2 10.0
625 sensorineural hearing loss 10.0
626 social phobia 10.0
627 chlamydia 10.0
628 inflammatory spondylopathy 10.0
629 cholera 10.0
630 endometrial adenocarcinoma 10.0
631 food allergy 10.0
632 pituitary adenoma 10.0
633 familial retinoblastoma 10.0
634 prostate disease 10.0
635 elephantiasis 10.0
636 scrapie 10.0
637 lymphopenia 10.0
638 spondylitis 10.0
639 muscular dystrophy 10.0
640 head injury 10.0
641 hepatitis c virus 10.0
642 tendinitis 10.0
643 angiosarcoma 10.0
644 hepatocellular adenoma 10.0
645 umbilical hernia 10.0
646 neuroretinitis 10.0
647 portal hypertension 10.0
648 microcephaly 10.0
649 pertussis 10.0
650 visual epilepsy 10.0
651 atypical depressive disorder 10.0
652 alcoholic hepatitis 10.0
653 leiomyoma 10.0
654 papilledema 10.0
655 pneumothorax 10.0
656 epilepsy 10.0
657 hepatitis 10.0
658 glomerulonephritis 10.0
659 retinitis 10.0
660 amyloidosis 10.0
661 heparin-induced thrombocytopenia 10.0
662 spondyloarthropathy 1 9.9
663 cardiac arrhythmia 9.9
664 pheochromocytoma 9.9
665 lipoid congenital adrenal hyperplasia 9.9
666 pancreatic agenesis 1 9.9
667 wilms tumor 5 9.9
668 tendinopathy 9.9
669 adrenal gland pheochromocytoma 9.9
670 inguinal hernia 9.9
671 aortic dissection 9.9
672 aortic atherosclerosis 9.9
673 renal hypertension 9.9
674 primary hyperparathyroidism 9.9
675 nephrosclerosis 9.9
676 dysthymic disorder 9.9
677 quadriplegia 9.9
678 severe pre-eclampsia 9.9
679 azoospermia 9.9
680 autoimmune hepatitis 9.9
681 eye disease 9.9
682 gastric cardia adenocarcinoma 9.9
683 dyskinesia of esophagus 9.9
684 cholangitis 9.9
685 developmental coordination disorder 9.9
686 substance dependence 9.9
687 hypoalphalipoproteinemia 9.9
688 central precocious puberty 9.9
689 developmental dyspraxia 9.9
690 pituitary tumors 9.9
691 cardiogenic shock 9.9
692 cleft palate, isolated 9.9
693 volvulus of midgut 9.9
694 wilms tumor 1 9.9
695 hemochromatosis, type 1 9.9
696 immune deficiency disease 9.9
697 branchiootic syndrome 1 9.9
698 ovarian hyperstimulation syndrome 9.9
699 aortic valve disease 2 9.9
700 aspiration pneumonia 9.9
701 restless legs syndrome 9.9
702 exanthem 9.9
703 estrogen-receptor positive breast cancer 9.9
704 microinvasive gastric cancer 9.9
705 borderline personality disorder 9.9
706 hydronephrosis 9.9
707 bipolar i disorder 9.9
708 generalized anxiety disorder 9.9
709 estrogen excess 9.9
710 panniculitis 9.9
711 hyperostosis 9.9
712 transient cerebral ischemia 9.9
713 papilloma 9.9
714 purpura 9.9
715 plague 9.9
716 thrombophlebitis 9.9
717 myopathy 9.9
718 neuromuscular disease 9.9
719 uremia 9.9
720 ovarian cyst 9.9
721 neuroblastoma 9.9
722 mediastinitis 9.9
723 vasculitis 9.9
724 pathologic nystagmus 9.9
725 placental abruption 9.9
726 periodontal ehlers-danlos syndrome 9.9
727 soft tissue sarcoma 9.9
728 syncope 9.9
729 tremor 9.9
730 sarcoidosis 1 9.9
731 small cell cancer of the lung 9.9
732 anencephaly 9.9
733 3-methylglutaconic aciduria, type iii 9.9
734 graves disease 1 9.9
735 ventricular fibrillation, paroxysmal familial, 1 9.9
736 carotid intimal medial thickness 2 9.9
737 preterm premature rupture of the membranes 9.9
738 cyanosis, transient neonatal 9.9
739 cholangiocarcinoma 9.9
740 chlamydia pneumonia 9.9
741 secondary progressive multiple sclerosis 9.9
742 idiopathic scoliosis 9.9
743 cerebral artery occlusion 9.9
744 blind loop syndrome 9.9
745 portal vein thrombosis 9.9
746 protein-energy malnutrition 9.9
747 primary biliary cirrhosis 9.9
748 squamous cell carcinoma 9.9
749 hypothalamic disease 9.9
750 exostosis 9.9
751 spondylosis 9.9
752 gastric adenocarcinoma 9.9
753 radiculopathy 9.9
754 myofibroma 9.9
755 movement disease 9.9
756 intrahepatic cholangiocarcinoma 9.9
757 agoraphobia 9.9
758 myocarditis 9.9
759 night blindness 9.9
760 fundus dystrophy 9.9
761 cleft lip 9.9
762 acute mountain sickness 9.9
763 antisynthetase syndrome 9.9
764 cerebral beriberi 9.9
765 inherited retinal disorder 9.9
766 acute liver failure 9.9
767 leukemia, chronic lymphocytic 9.9
768 tetralogy of fallot 9.9
769 urate oxidase, pseudogene 9.9
770 myasthenia gravis 9.9
771 thymoma, familial 9.9
772 suppression of tumorigenicity 12 9.9
773 huntington disease-like 1 9.9
774 aspirin resistance 9.9
775 hypertension, diastolic 9.9
776 congenital hypothyroidism 9.9
777 familial adenomatous polyposis 9.9
778 brachydactyly 9.9
779 female breast cancer 9.9
780 ptosis 9.9
781 adenoid hypertrophy 9.9
782 short bowel syndrome 9.9
783 asphyxia neonatorum 9.9
784 choledocholithiasis 9.9
785 varicocele 9.9
786 tuberous sclerosis 9.9
787 gonadal dysgenesis 9.9
788 prostatitis 9.9
789 rectum adenocarcinoma 9.9
790 astrocytoma 9.9
791 interstitial lung disease 9.9
792 thymoma 9.9
793 breast disease 9.9
794 turner syndrome 9.9
795 borna disease 9.9
796 central sleep apnea 9.9
797 exophthalmos 9.9
798 plantar fasciitis 9.9
799 necrotizing fasciitis 9.9
800 hemophilia 9.9
801 acute graft versus host disease 9.9
802 aniridia 1 9.8
803 scoliosis, isolated 1 9.8
804 tuberous sclerosis 1 9.8
805 ascites, chylous 9.8
806 spondylometaphyseal dysplasia, sedaghatian type 9.8
807 pituitary hormone deficiency, combined, 2 9.8
808 mycobacterium tuberculosis 1 9.8
809 leukemia, chronic myeloid 9.8
810 phobia, specific 9.8
811 microphthalmia, syndromic 10 9.8
812 body mass index quantitative trait locus 13 9.8
813 aspergillosis 9.8
814 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 9.8
815 glucocorticoid resistance, generalized 9.8
816 hyperproinsulinemia 9.8
817 familial partial lipodystrophy 9.8
818 hyperphosphatemia 9.8
819 androgenic alopecia 9.8
820 colon adenoma 9.8
821 crohn's colitis 9.8
822 myelomeningocele 9.8
823 ectopic pregnancy 9.8
824 pollen allergy 9.8
825 familial glucocorticoid deficiency 9.8
826 sarcoma 9.8
827 cholecystolithiasis 9.8
828 cauda equina syndrome 9.8
829 oligohydramnios 9.8
830 urticaria 9.8
831 colon adenocarcinoma 9.8
832 cystadenoma 9.8
833 glycogen storage disease 9.8
834 gastric dilatation 9.8
835 teratoma 9.8
836 fibrosarcoma 9.8
837 liposarcoma 9.8
838 tricuspid valve insufficiency 9.8
839 hypertrichosis 9.8
840 spindle cell sarcoma 9.8
841 lymphocele 9.8
842 intestinal disease 9.8
843 aortic valve insufficiency 9.8
844 polyhydramnios 9.8
845 chronic fatigue syndrome 9.8
846 meningitis 9.8
847 encephalitis 9.8
848 pulmonary emphysema 9.8
849 myotonic dystrophy 9.8
850 brain tumor, childhood 9.8
851 cerebrospinal fluid leak 9.8
852 mast cell activation syndrome 9.8
853 pediatric multiple sclerosis 9.8
854 angelman syndrome 9.8
855 glaucoma, primary open angle 9.8
856 lipomatosis, multiple symmetric 9.8
857 lipomatosis, multiple 9.8
858 neutrophil migration 9.8
859 pilonidal sinus 9.8
860 chromosome 2q35 duplication syndrome 9.8
861 wolfram syndrome 1 9.8
862 enterocolitis 9.8
863 myxedema 9.8
864 platelet glycoprotein iv deficiency 9.8
865 human immunodeficiency virus type 1 9.8
866 acute promyelocytic leukemia 9.8
867 peripartum cardiomyopathy 9.8
868 chronic ulcer of skin 9.8
869 oppositional defiant disorder 9.8
870 follicular lymphoma 9.8
871 pelvic inflammatory disease 9.8
872 osteomyelitis 9.8
873 pleomorphic lipoma 9.8
874 meningoencephalitis 9.8
875 open-angle glaucoma 9.8
876 thrombotic thrombocytopenic purpura 9.8
877 hypospadias 9.8
878 depersonalization disorder 9.8
879 meconium aspiration syndrome 9.8
880 placenta praevia 9.8
881 hemopericardium 9.8
882 mitral valve insufficiency 9.8
883 pericardial effusion 9.8
884 bile reflux 9.8
885 hypochondriasis 9.8
886 hyperinsulinemic hypoglycemia 9.8
887 premature ejaculation 9.8
888 cystitis 9.8
889 heart septal defect 9.8
890 optic nerve disease 9.8
891 gastroenteritis 9.8
892 sensory peripheral neuropathy 9.8
893 pulmonary tuberculosis 9.8
894 mediastinal lipomatosis 9.8
895 folliculitis 9.8
896 calciphylaxis 9.8
897 neurotic disorder 9.8
898 adjustment disorder 9.8
899 colonic disease 9.8
900 acute pyelonephritis 9.8
901 adrenal adenoma 9.8
902 juvenile rheumatoid arthritis 9.8
903 monoclonal gammopathy of uncertain significance 9.8
904 active peptic ulcer disease 9.8
905 childhood leukemia 9.8
906 osteochondrosis 9.8
907 subacute delirium 9.8
908 decubitus ulcer 9.8
909 bacterial pneumonia 9.8
910 atrophic gastritis 9.8
911 kidney hypertrophy 9.8
912 disorders of gnas inactivation 9.8
913 amyloidosis aa 9.8
914 encephalocele 9.8
915 glioma 9.8
916 prosthetic joint infection 9.8
917 pure autonomic failure 9.8
918 splenomegaly 9.8
919 clopidogrel resistance 9.8
920 opioid addiction 9.8
921 posttransplant acute limbic encephalitis 9.8
922 glial tumor 9.8
923 pouchitis 9.8
924 acute sensory ataxic neuropathy 9.8
925 progressive familial heart block, type ia 9.7
926 maturity-onset diabetes of the young, type 1 9.7
927 macroglossia 9.7
928 meralgia paraesthetica, familial 9.7
929 strabismus 9.7
930 thyroid cancer, nonmedullary, 1 9.7
931 acrocallosal syndrome 9.7
932 adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency 9.7
933 central hypoventilation syndrome, congenital 9.7
934 osteogenic sarcoma 9.7
935 phenylketonuria 9.7
936 abnormal hair, joint laxity, and developmental delay 9.7
937 lysosomal acid lipase deficiency 9.7
938 paine syndrome 9.7
939 androgen insensitivity, partial 9.7
940 pituitary adenoma, prolactin-secreting 9.7
941 chudley-mccullough syndrome 9.7
942 asthma-related traits 4 9.7
943 lung cancer susceptibility 3 9.7
944 myelodysplastic syndrome 9.7
945 juvenile arthritis 9.7
946 hypophosphatemia 9.7
947 small cell carcinoma 9.7
948 colorectal adenocarcinoma 9.7
949 withdrawal disorder 9.7
950 omphalocele 9.7
951 drug allergy 9.7
952 polycystic kidney disease 9.7
953 migraine with aura 9.7
954 t cell deficiency 9.7
955 disseminated intravascular coagulation 9.7
956 adult respiratory distress syndrome 9.7
957 diabetic autonomic neuropathy 9.7
958 pica disease 9.7
959 guillain-barre syndrome 9.7
960 megaesophagus 9.7
961 kwashiorkor 9.7
962 somatization disorder 9.7
963 alcoholic liver cirrhosis 9.7
964 renal tubular acidosis 9.7
965 sclerosing cholangitis 9.7
966 ventricular septal defect 9.7
967 cardiovascular cancer 9.7
968 post-thrombotic syndrome 9.7
969 hemangioma 9.7
970 tic disorder 9.7
971 acquired polycythemia 9.7
972 long qt syndrome 9.7
973 bronchiolitis 9.7
974 cystic kidney disease 9.7
975 antiphospholipid syndrome 9.7
976 tracheal stenosis 9.7
977 histiocytosis 9.7
978 pleural empyema 9.7
979 placental insufficiency 9.7
980 esophagus adenocarcinoma 9.7
981 dystonia 9.7
982 adult acute lymphocytic leukemia 9.7
983 thyroid hyalinizing trabecular adenoma 9.7
984 acquired immunodeficiency syndrome 9.7
985 peroneal nerve paralysis 9.7
986 premenstrual tension 9.7
987 measles 9.7
988 duodenitis 9.7
989 perinatal necrotizing enterocolitis 9.7
990 in situ carcinoma 9.7
991 dermatophytosis 9.7
992 cervix uteri carcinoma in situ 9.7
993 gas gangrene 9.7
994 homocystinuria 9.7
995 mechanical strabismus 9.7
996 status asthmaticus 9.7
997 biliary tract disease 9.7
998 isolated gonadotropin-releasing hormone deficiency 9.7
999 multiple epiphyseal dysplasia, recessive 9.7
1000 cervical intraepithelial neoplasia 9.7
1001 congenital hypopituitarism 9.7
1002 familial hypertension 9.7
1003 fournier gangrene 9.7
1004 hair-an syndrome 9.7
1005 tuberculous meningitis 9.7
1006 abdominal wall defect 9.7
1007 bunion 9.7
1008 cytomegalovirus infection 9.7
1009 cleft lip/palate 9.7
1010 cerebrofacial arteriovenous metameric syndrome 9.7
1011 inflammatory myopathy with abundant macrophages 9.7
1012 thyroid tumor 9.7
1013 pfeiffer syndrome 9.7
1014 amyotrophic lateral sclerosis 1 9.7
1015 coarctation of aorta 9.7
1016 coffin-siris syndrome 1 9.7
1017 hypertelorism 9.7
1018 kaposi sarcoma 9.7
1019 lichen sclerosus et atrophicus 9.7
1020 lipodystrophy, familial partial, type 2 9.7
1021 parkinson disease, late-onset 9.7
1022 polykaryocytosis inducer 9.7
1023 dowling-degos disease 1 9.7
1024 spondylosis, cervical 9.7
1025 digeorge syndrome 9.7
1026 suppressor of tumorigenicity 3 9.7
1027 renal hypodysplasia/aplasia 1 9.7
1028 vesicoureteral reflux 1 9.7
1029 galactorrhea 9.7
1030 niemann-pick disease, type c1 9.7
1031 fragile x syndrome 9.7
1032 hemophilia a 9.7
1033 muscular dystrophy, duchenne type 9.7
1034 otopalatodigital syndrome, type i 9.7
1035 kearns-sayre syndrome 9.7
1036 retinitis pigmentosa 11 9.7
1037 frontotemporal dementia 9.7
1038 intervertebral disc disease 9.7
1039 mammographic density 9.7
1040 myopathy, myosin storage, autosomal dominant 9.7
1041 coronary heart disease 7 9.7
1042 intraocular pressure quantitative trait locus 9.7
1043 alpha-1-antitrypsin deficiency 9.7
1044 complement component 3 deficiency, autosomal recessive 9.7
1045 cholangitis, primary sclerosing 9.7
1046 fanconi anemia, complementation group l 9.7
1047 dengue virus 9.7
1048 accelerated tumor formation 9.7
1049 pachyonychia congenita 3 9.7
1050 hydrops, lactic acidosis, and sideroblastic anemia 9.7
1051 joint laxity, short stature, and myopia 9.7
1052 orofacial cleft 9.7
1053 paraganglioma 9.7
1054 cone dystrophy 9.7
1055 infective endocarditis 9.7
1056 body dysmorphic disorder 9.7
1057 dextro-looped transposition of the great arteries 9.7
1058 isolated growth hormone deficiency 9.7
1059 keratoconus 9.7
1060 xerophthalmia 9.7
1061 endocarditis 9.7
1062 tonsillitis 9.7
1063 nasopharyngitis 9.7
1064 cardia cancer 9.7
1065 microphthalmia 9.7
1066 salivary gland disease 9.7
1067 multiple personality disorder 9.7
1068 antisocial personality disorder 9.7
1069 hemiplegia 9.7
1070 esophageal varix 9.7
1071 rabies 9.7
1072 tetanus 9.7
1073 megacolon 9.7
1074 penile cancer 9.7
1075 cornelia de lange syndrome 9.7
1076 lyme disease 9.7
1077 myopia 9.7
1078 coronary thrombosis 9.7
1079 chagas disease 9.7
1080 neurogenic bladder 9.7
1081 dengue hemorrhagic fever 9.7
1082 paranoid schizophrenia 9.7
1083 graves' disease 9.7
1084 dysentery 9.7
1085 pathological gambling 9.7
1086 pancytopenia 9.7
1087 hepatic coma 9.7
1088 diabetic polyneuropathy 9.7
1089 keratoconjunctivitis sicca 9.7
1090 carotid stenosis 9.7
1091 uveitis 9.7
1092 exocrine pancreatic insufficiency 9.7
1093 diabetic cataract 9.7
1094 megaloblastic anemia 9.7
1095 hepatic encephalopathy 9.7
1096 patent foramen ovale 9.7
1097 squamous cell papilloma 9.7
1098 bacteriuria 9.7
1099 niemann-pick disease 9.7
1100 endogenous depression 9.7
1101 neuroendocrine tumor 9.7
1102 ocular melanoma 9.7
1103 mitral valve stenosis 9.7
1104 pericarditis 9.7
1105 status epilepticus 9.7
1106 lateral sclerosis 9.7
1107 neonatal jaundice 9.7
1108 gangliocytoma 9.7
1109 cystic teratoma 9.7
1110 myoma 9.7
1111 anuria 9.7
1112 glioblastoma multiforme 9.7
1113 aspiration pneumonitis 9.7
1114 carotid artery disease 9.7
1115 duodenal obstruction 9.7
1116 lynch syndrome 9.7
1117 ganglioneuroma 9.7
1118 poliomyelitis 9.7
1119 arteriolosclerosis 9.7
1120 urinary tract obstruction 9.7
1121 ovarian serous cystadenocarcinoma 9.7
1122 conjunctivitis 9.7
1123 inflammatory breast carcinoma 9.7
1124 juvenile pilocytic astrocytoma 9.7
1125 complement component 3 deficiency 9.7
1126 paralytic ileus 9.7
1127 choline deficiency disease 9.7
1128 chickenpox 9.7
1129 skin melanoma 9.7
1130 dacryoadenitis 9.7
1131 polyarteritis nodosa 9.7
1132 mitochondrial disorders 9.7
1133 sickle cell disease 9.7
1134 autoimmune encephalitis 9.7
1135 biliary tract cancer 9.7
1136 carcinoma showing thymus-like differentiation 9.7
1137 chromosome 15q deletion 9.7
1138 cluster headache 9.7
1139 fasting hypoglycemia 9.7
1140 single ventricular heart 9.7
1141 sudden sensorineural hearing loss 9.7
1142 anoxia 9.7
1143 cerebral atrophy 9.7
1144 dysautonomia 9.7
1145 foot drop 9.7
1146 hypertonia 9.7
1147 infantile hypotonia 9.7
1148 perioral myoclonia with absences 9.7
1149 periodic paralysis 9.7
1150 virus-associated trichodysplasia spinulosa 9.7
1151 malignant tumor of penis 9.7
1152 benign idiopathic neonatal seizures 9.7
1153 primary lymphedema 9.7
1154 maternal uniparental disomy 9.7
1155 cerebral amyloid angiopathy, cst3-related 9.6
1156 blood group--newfoundland 9.6
1157 cardiomyopathy, familial hypertrophic, 2 9.6
1158 coloboma of macula 9.6
1159 cornelia de lange syndrome 1 9.6
1160 diabetes mellitus, insulin-dependent, 2 9.6
1161 earlobe crease 9.6
1162 beckwith-wiedemann syndrome 9.6
1163 lateral meningocele syndrome 9.6
1164 erythermalgia, primary 9.6
1165 gilles de la tourette syndrome 9.6
1166 hand skill, relative 9.6
1167 diaphragmatic hernia, congenital 9.6
1168 laryngomalacia 9.6
1169 legg-calve-perthes disease 9.6
1170 myositis 9.6
1171 neutrophilia, hereditary 9.6
1172 optic nerve hypoplasia, bilateral 9.6
1173 pancreas, dorsal, agenesis of 9.6
1174 papillomatosis, confluent and reticulated 9.6
1175 retinal detachment 9.6
1176 syringomyelia, noncommunicating isolated 9.6
1177 temporal arteritis 9.6
1178 thrombophilia due to activated protein c resistance 9.6
1179 trigeminal neuralgia 9.6
1180 williams-beuren syndrome 9.6
1181 joubert syndrome 1 9.6
1182 schopf-schulz-passarge syndrome 9.6
1183 enterokinase deficiency 9.6
1184 gastroschisis 9.6
1185 hyperlipoproteinemia, type i 9.6
1186 leprosy 3 9.6
1187 chylomicron retention disease 9.6
1188 methane production 9.6
1189 multiple pterygium syndrome, lethal type 9.6
1190 polycythemia vera 9.6
1191 short syndrome 9.6
1192 sjogren syndrome 9.6
1193 asplenia, isolated congenital 9.6
1194 sudden infant death syndrome 9.6
1195 hypothyroidism, congenital, nongoitrous, 4 9.6
1196 wernicke-korsakoff syndrome 9.6
1197 mental retardation-hypotonic facies syndrome, x-linked, 1 9.6
1198 rett syndrome 9.6
1199 maturity-onset diabetes of the young, type 3 9.6
1200 abcd syndrome 9.6
1201 leptin, serum level of, quantitative trait locus 1 9.6
1202 astigmatism 9.6
1203 pseudohypoparathyroidism, type ib 9.6
1204 brittle bone disorder 9.6
1205 sickle cell anemia 9.6
1206 progressive familial heart block, type ib 9.6
1207 langerhans cell histiocytosis 9.6
1208 anisomastia 9.6
1209 alveolar soft part sarcoma 9.6
1210 niemann-pick disease, type c2 9.6
1211 chromosome 1p36 deletion syndrome 9.6
1212 hypertensive nephropathy 9.6
1213 kala-azar 1 9.6
1214 asthma-related traits 2 9.6
1215 testicular microlithiasis 9.6
1216 malaria 9.6
1217 cavitary optic disc anomalies 9.6
1218 kawasaki disease 9.6
1219 chromosome 16p11.2 deletion syndrome, 593-kb 9.6
1220 antithrombin iii deficiency 9.6
1221 plasminogen activator inhibitor-1 deficiency 9.6
1222 myxoid liposarcoma 9.6
1223 macrostomia, isolated 9.6
1224 glycerol quantitative trait locus 9.6
1225 ras-associated autoimmune leukoproliferative disorder 9.6
1226 bainbridge-ropers syndrome 9.6
1227 alkuraya-kucinskas syndrome 9.6
1228 neuropathy, congenital hypomyelinating, 2 9.6
1229 hypertrophic scars 9.6
1230 tendinosis 9.6
1231 bacterial sepsis 9.6
1232 autoimmune peripheral neuropathy 9.6
1233 invasive aspergillosis 9.6
1234 asperger syndrome 9.6
1235 distal arthrogryposis 9.6
1236 fetal alcohol syndrome 9.6
1237 fetal alcohol spectrum disorder 9.6
1238 zollinger-ellison syndrome 9.6
1239 atrioventricular block 9.6
1240 hemorrhagic cystitis 9.6
1241 fibroma 9.6
1242 pancreatic agenesis 9.6
1243 interleukin-7 receptor alpha deficiency 9.6
1244 pervasive developmental disorder 9.6
1245 microscopic colitis 9.6
1246 ileitis 9.6
1247 ileocolitis 9.6
1248 stuttering 9.6
1249 tracheomalacia 9.6
1250 anal fistula 9.6
1251 transient neonatal diabetes mellitus 9.6
1252 spinal disease 9.6
1253 myoglobinuria 9.6
1254 lymphoblastic lymphoma 9.6
1255 benign teratoma 9.6
1256 type 1 diabetes mellitus 2 9.6
1257 endometrial disease 9.6
1258 cysticercosis 9.6
1259 osteonecrosis 9.6
1260 left bundle branch hemiblock 9.6
1261 lactose intolerance 9.6
1262 interstitial nephritis 9.6
1263 wolfram syndrome 9.6
1264 chronic pyelonephritis 9.6
1265 obsessive-compulsive personality disorder 9.6
1266 brucellosis 9.6
1267 allergic conjunctivitis 9.6
1268 spondyloarthropathy 9.6
1269 microcytic anemia 9.6
1270 erysipelas 9.6
1271 constrictive pericarditis 9.6
1272 neonatal diabetes mellitus 9.6
1273 mononeuropathy 9.6
1274 lymphocytic choriomeningitis 9.6
1275 bronchopneumonia 9.6
1276 spinal muscular atrophy 9.6
1277 hepatitis a 9.6
1278 acute kidney tubular necrosis 9.6
1279 nephrocalcinosis 9.6
1280 newborn respiratory distress syndrome 9.6
1281 telangiectasis 9.6
1282 migraine without aura 9.6
1283 endomyocardial fibrosis 9.6
1284 renal osteodystrophy 9.6
1285 hellp syndrome 9.6
1286 right bundle branch block 9.6
1287 osteopetrosis 9.6
1288 obstructive jaundice 9.6
1289 biliary atresia 9.6
1290 sick sinus syndrome 9.6
1291 epicondylitis 9.6
1292 familial lipoprotein lipase deficiency 9.6
1293 oligospermia 9.6
1294 pyuria 9.6
1295 hypersensitivity reaction type iii disease 9.6
1296 angioedema 9.6
1297 rheumatic fever 9.6
1298 renovascular hypertension 9.6
1299 calcinosis 9.6
1300 urethral stricture 9.6
1301 dysostosis 9.6
1302 thrombocytosis 9.6
1303 ankylosis 9.6
1304 craniosynostosis 9.6
1305 basal cell carcinoma 9.6
1306 testicular disease 9.6
1307 hematologic cancer 9.6
1308 transitional cell carcinoma 9.6
1309 lymphangiosarcoma 9.6
1310 phimosis 9.6
1311 endocrine system disease 9.6
1312 cranial nerve malignant neoplasm 9.6
1313 cervix carcinoma 9.6
1314 papillary carcinoma 9.6
1315 multiple endocrine neoplasia 9.6
1316 scleredema adultorum 9.6
1317 neurilemmoma 9.6
1318 demyelinating disease 9.6
1319 myelitis 9.6
1320 syringomyelia 9.6
1321 germinoma 9.6
1322 temporal lobe epilepsy 9.6
1323 bone inflammation disease 9.6
1324 bacterial vaginosis 9.6
1325 laryngitis 9.6
1326 mammary paget's disease 9.6
1327 breast adenocarcinoma 9.6
1328 necrobiosis lipoidica 9.6
1329 mastocytosis 9.6
1330 mast cell neoplasm 9.6
1331 pulmonary fibrosis 9.6
1332 male reproductive organ cancer 9.6
1333 restrictive cardiomyopathy 9.6
1334 duodenogastric reflux 9.6
1335 ganglioneuroblastoma 9.6
1336 pyoderma 9.6
1337 dyslexia 9.6
1338 holoprosencephaly 9.6
1339 extracutaneous mastocytoma 9.6
1340 brain edema 9.6
1341 essential tremor 9.6
1342 arteriosclerosis obliterans 9.6
1343 demyelinating polyneuropathy 9.6
1344 mature teratoma 9.6
1345 hemolytic anemia 9.6
1346 connective tissue disease 9.6
1347 diffuse idiopathic skeletal hyperostosis 9.6
1348 delusional disorder 9.6
1349 gallbladder melanoma 9.6
1350 brachial plexus lesion 9.6
1351 pellagra 9.6
1352 neurofibromatosis 9.6
1353 rosacea 9.6
1354 autosomal dominant polycystic kidney disease 9.6
1355 leishmaniasis 9.6
1356 ocular hypertension 9.6
1357 tracheitis 9.6
1358 lipid storage disease 9.6
1359 uterine corpus cancer 9.6
1360 bronchiectasis 9.6
1361 hydrocele 9.6
1362 toxoplasmosis 9.6
1363 16p11.2 recurrent microdeletion 9.6
1364 bap1 tumor predisposition syndrome 9.6
1365 hypermobile ehlers-danlos syndrome 9.6
1366 chiari malformation 9.6
1367 complete androgen insensitivity syndrome 9.6
1368 germ cells tumors 9.6
1369 gigantism 9.6
1370 glucagonoma 9.6
1371 hansen's disease 9.6
1372 lymphomatous thyroiditis 9.6
1373 neural crest tumor 9.6
1374 pituitary stalk interruption syndrome 9.6
1375 pseudobulbar affect 9.6
1376 transverse myelitis 9.6
1377 raynaud phenomenon 9.6
1378 aldosterone-producing adenoma 9.6
1379 cerebral hypoxia 9.6
1380 febrile seizures 9.6
1381 idiopathic central precocious puberty 9.6
1382 differentiated thyroid carcinoma 9.6
1383 uniparental disomy of chromosome 15 9.6
1384 uniparental disomy of chromosome 1 9.6
1385 severe early-childhood-onset retinal dystrophy 9.6
1386 arterial thoracic outlet syndrome 9.6
1387 paracetamol poisoning 9.6
1388 chronic enteropathy associated with slco2a1 gene 9.6
1389 avascular necrosis 9.6
1390 necrotizing soft tissue infection 9.6
1391 congenital amyoplasia 9.6
1392 serotonin syndrome 9.6
1393 non-specific syndromic intellectual disability 9.6
1394 rare tumor 9.6
1395 acth-independent cushing syndrome 9.6
1396 abducens palsy 9.4
1397 anisocoria 9.4
1398 arteriovenous malformations of the brain 9.4
1399 machado-joseph disease 9.4
1400 brachydactyly-nystagmus-cerebellar ataxia 9.4
1401 sotos syndrome 1 9.4
1402 chiari malformation type i 9.4
1403 corneal dystrophy, epithelial basement membrane 9.4
1404 creutzfeldt-jakob disease 9.4
1405 dens evaginatus 9.4
1406 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.4
1407 major affective disorder 1 9.4
1408 multiple endocrine neoplasia, type i 9.4
1409 camurati-engelmann disease 9.4
1410 pilomatrixoma 9.4
1411 exostoses, multiple, type ii 9.4
1412 lymphoma, mucosa-associated lymphoid type 9.4
1413 hemifacial spasm, familial 9.4
1414 congenital anomalies of kidney and urinary tract 2 9.4
1415 hyperalphalipoproteinemia 1 9.4
1416 gilbert syndrome 9.4
1417 hyperlipoproteinemia, type iv 9.4
1418 hyperparathyroidism 1 9.4
1419 hypogonadotropic hypogonadism 7 with or without anosmia 9.4
1420 multiple system atrophy 1 9.4
1421 keloid formation 9.4
1422 leiomyoma, uterine 9.4
1423 lentigines 9.4
1424 li-fraumeni syndrome 9.4
1425 marfan syndrome 9.4
1426 thyroid carcinoma, familial medullary 9.4
1427 medulloblastoma 9.4
1428 melanoma, uveal 9.4
1429 metaphyseal chondrodysplasia, schmid type 9.4
1430 moebius syndrome 9.4
1431 nondisjunction 9.4
1432 motion sickness 9.4
1433 cowden syndrome 1 9.4
1434 noonan syndrome 1 9.4
1435 osseous heteroplasia, progressive 9.4
1436 andersen cardiodysrhythmic periodic paralysis 9.4
1437 hypokalemic periodic paralysis, type 1 9.4
1438 platelet membrane fluidity 9.4
1439 hutchinson-gilford progeria syndrome 9.4
1440 pulmonary fibrosis, idiopathic 9.4
1441 pulmonary hemosiderosis 9.4
1442 raynaud disease 9.4
1443 schistosoma mansoni infection, susceptibility/ 9.4
1444 spinocerebellar ataxia 2 9.4
1445 odontochondrodysplasia 9.4
1446 stiff-person syndrome 9.4
1447 thrombocytopenic purpura, autoimmune 9.4
1448 trichorhinophalangeal syndrome, type i 9.4
1449 uterine anomalies 9.4
1450 cardiomyopathy, familial hypertrophic, 1 9.4
1451 vitiligo-associated multiple autoimmune disease susceptibility 6 9.4
1452 wolf-hirschhorn syndrome 9.4
1453 acyl-coa dehydrogenase, short-chain, deficiency of 9.4
1454 adrenocortical carcinoma, hereditary 9.4
1455 tangier disease 9.4
1456 arterial tortuosity syndrome 9.4
1457 ataxia-telangiectasia 9.4
1458 cardiomyopathy, dilated, with hypergonadotropic hypogonadism 9.4
1459 congenital heart defects, hamartomas of tongue, and polysyndactyly 9.4
1460 corpus callosum, agenesis of 9.4
1461 costello syndrome 9.4
1462 craniosynostosis with fibular aplasia 9.4
1463 mitochondrial complex iv deficiency 9.4
1464 leukoencephalopathy, hereditary diffuse, with spheroids 9.4
1465 diastrophic dysplasia 9.4
1466 duodenal atresia 9.4
1467 ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive 9.4
1468 fanconi anemia, complementation group c 9.4
1469 fanconi anemia, complementation group a 9.4
1470 fructose utilization 9.4
1471 gaucher disease, type i 9.4
1472 multiple acyl-coa dehydrogenase deficiency 9.4
1473 halothane hepatitis 9.4
1474 hydrocephalus, congenital, 1 9.4
1475 hydrocephalus due to congenital stenosis of aqueduct of sylvius 9.4
1476 hypoadrenocorticism, familial 9.4
1477 autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia 9.4
1478 cholestasis, benign recurrent intrahepatic, 1 9.4
1479 succinyl-coa:3-oxoacid-coa transferase deficiency 9.4
1480 laryngoonychocutaneous syndrome 9.4
1481 laurence-moon syndrome 9.4
1482 familial mediterranean fever 9.4
1483 spinal muscular atrophy, type iii 9.4
1484 myeloperoxidase deficiency 9.4
1485 myopathy, myosin storage, autosomal recessive 9.4
1486 neuraminidase deficiency 9.4
1487 hyperoxaluria, primary, type i 9.4
1488 hyperoxaluria, primary, type ii 9.4
1489 short-rib thoracic dysplasia 6 with or without polydactyly 9.4
1490 pulmonic stenosis 9.4
1491 pycnodysostosis 9.4
1492 inflammatory bowel disease 1 9.4
1493 respiratory distress syndrome in premature infants 9.4
1494 sodium-potassium-atpase activity of red cell 9.4
1495 spermatogenic failure 4 9.4
1496 succinic semialdehyde dehydrogenase deficiency 9.4
1497 taurodontism 9.4
1498 thyrotropin-releasing hormone deficiency 9.4
1499 hypothyroidism, congenital, nongoitrous, 1 9.4
1500 chanarin-dorfman syndrome 9.4
1501 werner syndrome 9.4
1502 wilson disease 9.4
1503 muscular dystrophy, becker type 9.4
1504 atkin-flaitz syndrome 9.4
1505 immunodeficiency 33 9.4
1506 cornelia de lange syndrome 5 9.4
1507 tubulin, beta 9.4
1508 choroideremia 9.4
1509 choroideremia, deafness, and mental retardation 9.4
1510 coffin-lowry syndrome 9.4
1511 deafness, x-linked 2 9.4
1512 glycerol kinase deficiency 9.4
1513 hypoparathyroidism, x-linked 9.4
1514 hypophosphatemic rickets, x-linked dominant 9.4
1515 mental retardation with optic atrophy, deafness, and seizures 9.4
1516 premature ovarian failure 1 9.4
1517 diabetes and deafness, maternally inherited 9.4
1518 oncocytoma 9.4
1519 gonadal agenesis 9.4
1520 fryns microphthalmia syndrome 9.4
1521 hypocalcemia, autosomal dominant 1 9.4
1522 amelia, posterior, with pelvic and pulmonary hypoplasia syndrome 9.4
1523 autoimmune lymphoproliferative syndrome 9.4
1524 suppressor of tumorigenicity 11 9.4
1525 ossification of the posterior longitudinal ligament of spine 9.4
1526 psoriasis 2 9.4
1527 bile duct cysts 9.4
1528 papillary thyroid microcarcinoma 9.4
1529 hypoalphalipoproteinemia, primary, 1 9.4
1530 mitochondrial complex v deficiency, nuclear type 1 9.4
1531 aceruloplasminemia 9.4
1532 rheumatoid arthritis, systemic juvenile 9.4
1533 orthostatic intolerance 9.4
1534 tricuspid atresia 9.4
1535 paragangliomas 3 9.4
1536 late-onset retinal degeneration 9.4
1537 fasting insulin level quantitative trait locus 1 9.4
1538 diamond-blackfan anemia 2 9.4
1539 atrioventricular septal defect 9.4
1540 maturity-onset diabetes of the young, type 4 9.4
1541 vitiligo-associated multiple autoimmune disease susceptibility 1 9.4
1542 lipodystrophy, familial partial, type 7 9.4
1543 spermatogenic failure 3 9.4
1544 adiponectin, serum level of, quantitative trait locus 2 9.4
1545 adiponectin, serum level of, quantitative trait locus 3 9.4
1546 nasopharyngeal carcinoma 9.4
1547 epilepsy, partial, with pericentral spikes 9.4
1548 asthma-related traits 1 9.4
1549 epidermolysis bullosa simplex superficialis 9.4
1550 peeling skin syndrome 4 9.4
1551 neutrophilic dermatosis, acute febrile 9.4
1552 tropical calcific pancreatitis 9.4
1553 slowed nerve conduction velocity, autosomal dominant 9.4
1554 parathyroid carcinoma 9.4
1555 coronary heart disease 4 9.4
1556 myocardial infarction 2 9.4
1557 lipodystrophy, congenital generalized, type 1 9.4
1558 transposition of the great arteries, dextro-looped 1 9.4
1559 carney complex variant 9.4
1560 telomere length, mean leukocyte 9.4
1561 aplastic anemia 9.4
1562 li-fraumeni syndrome 2 9.4
1563 syndactyly, mesoaxial synostotic, with phalangeal reduction 9.4
1564 esophagitis, eosinophilic, 1 9.4
1565 potocki-lupski syndrome 9.4
1566 skin/hair/eye pigmentation, variation in, 9 9.4
1567 alopecia, neurologic defects, and endocrinopathy syndrome 9.4
1568 trehalase deficiency 9.4
1569 myd88 deficiency 9.4
1570 joubert syndrome 8 9.4
1571 lipodystrophy, congenital generalized, type 3 9.4
1572 microvascular complications of diabetes 2 9.4
1573 polymicrogyria, bilateral temporooccipital 9.4
1574 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.4
1575 premature ovarian failure 7 9.4
1576 hearing loss, noise-induced 9.4
1577 trichotillomania 9.4
1578 tuberous sclerosis 2 9.4
1579 brachydactyly, type e2 9.4
1580 autism 17 9.4
1581 cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 9.4
1582 membranous nephropathy 9.4
1583 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 9.4
1584 monocarboxylate transporter 1 deficiency 9.4
1585 chronic mountain sickness 9.4
1586 seizures, scoliosis, and macrocephaly/microcephaly syndrome 9.4
1587 chorea, childhood-onset, with psychomotor retardation 9.4
1588 nevus comedonicus 9.4
1589 short stature, developmental delay, and congenital heart defects 9.4
1590 aniridia 2 9.4
1591 renal hypodysplasia/aplasia 3 9.4
1592 central centrifugal cicatricial alopecia 9.4
1593 fetal akinesia deformation sequence 3 9.4
1594 adrenal cortical carcinoma 9.4
1595 autoimmune uveitis 9.4
1596 autoimmune gastritis 9.4
1597 chikungunya 9.4
1598 dengue shock syndrome 9.4
1599 tick-borne encephalitis 9.4
1600 arrhythmogenic right ventricular cardiomyopathy 9.4
1601 periventricular nodular heterotopia 9.4
1602 multinodular goiter 9.4
1603 congenital generalized lipodystrophy 9.4
1604 severe congenital neutropenia 9.4
1605 tooth agenesis 9.4
1606 extrapulmonary tuberculosis 9.4
1607 hypochromic microcytic anemia 9.4
1608 alcohol-related birth defect 9.4
1609 spastic cerebral palsy 9.4
1610 mantle cell lymphoma 9.4
1611 third-degree atrioventricular block 9.4
1612 sinoatrial node disease 9.4
1613 oral squamous cell carcinoma 9.4
1614 adrenal cortical adenoma 9.4
1615 gastrointestinal carcinoma 9.4
1616 ovarian serous carcinoma 9.4
1617 munchausen by proxy 9.4
1618 ductal carcinoma in situ 9.4
1619 estrogen-receptor negative breast cancer 9.4
1620 gamma-amino butyric acid metabolism disorder 9.4
1621 ischemic colitis 9.4
1622 clostridium difficile colitis 9.4
1623 sclerosteosis 9.4
1624 autosomal dominant non-syndromic intellectual disability 9.4
1625 lung abscess 9.4
1626 respiratory allergy 9.4
1627 autoimmune neuropathy 9.4
1628 penicillin allergy 9.4
1629 hyperekplexia 9.4
1630 autosomal dominant non-syndromic intellectual disability 1 9.4
1631 progressive familial intrahepatic cholestasis 9.4
1632 mucositis 9.4
1633 chronic myelomonocytic leukemia 9.4
1634 superior semicircular canal dehiscence 9.4
1635 cakut 9.4
1636 nodal marginal zone lymphoma 9.4
1637 mixed sleep apnea 9.4
1638 bronchiectasis 3 9.4
1639 tongue carcinoma 9.4
1640 rasopathy 9.4
1641 nodular malignant melanoma 9.4
1642 pigmentation disease 9.4
1643 thymus lymphoma 9.4
1644 pleurisy 9.4
1645 mumps 9.4
1646 monocular esotropia 9.4
1647 siderosis 9.4
1648 blepharophimosis 9.4
1649 common cold 9.4
1650 esophageal atresia 9.4
1651 viral pneumonia 9.4
1652 supine hypotensive syndrome 9.4
1653 charcot-marie-tooth disease 9.4
1654 protein-losing enteropathy 9.4
1655 frontal sinusitis 9.4
1656 malignant hypertension 9.4
1657 voyeurism 9.4
1658 abducens nerve disease 9.4
1659 benign essential hypertension 9.4
1660 amnestic disorder 9.4
1661 impulse control disorder 9.4
1662 myiasis 9.4
1663 enophthalmos 9.4
1664 hypoparathyroidism 9.4
1665 opioid abuse 9.4
1666 appendix cancer 9.4
1667 arteriovenous malformation 9.4
1668 retinal microaneurysm 9.4
1669 schizophreniform disorder 9.4
1670 gingival recession 9.4
1671 functional diarrhea 9.4
1672 alternating exotropia 9.4
1673 exotropia 9.4
1674 sciatic neuropathy 9.4
1675 autonomic nervous system disease 9.4
1676 horner's syndrome 9.4
1677 suppurative otitis media 9.4
1678 rumination disorder 9.4
1679 hypertensive retinopathy 9.4
1680 emery-dreifuss muscular dystrophy 9.4
1681 chronic laryngitis 9.4
1682 hepatorenal syndrome 9.4
1683 clubfoot 9.4
1684 tinea cruris 9.4
1685 synostosis 9.4
1686 pulmonary alveolar proteinosis 9.4
1687 common variable immunodeficiency 9.4
1688 descending colon cancer 9.4
1689 dengue disease 9.4
1690 anisometropia 9.4
1691 cough variant asthma 9.4
1692 marasmus 9.4
1693 endocrine exophthalmos 9.4
1694 entropion 9.4
1695 intermittent explosive disorder 9.4
1696 tinea pedis 9.4
1697 hemolytic-uremic syndrome 9.4
1698 acoustic neuroma 9.4
1699 cerebral atherosclerosis 9.4
1700 ancylostomiasis 9.4
1701 choreatic disease 9.4
1702 miller fisher syndrome 9.4
1703 sialolithiasis 9.4
1704 central nervous system leukemia 9.4
1705 hereditary spherocytosis 9.4
1706 leukostasis 9.4
1707 vertebrobasilar insufficiency 9.4
1708 balanitis 9.4
1709 mechanical entropion 9.4
1710 crescentic glomerulonephritis 9.4
1711 esophageal candidiasis 9.4
1712 allergic bronchopulmonary aspergillosis 9.4
1713 brain cancer 9.4
1714 nontoxic goiter 9.4
1715 nodular goiter 9.4
1716 intestinal tuberculosis 9.4
1717 congenital toxoplasmosis 9.4
1718 ehlers-danlos syndrome 9.4
1719 neurosarcoidosis 9.4
1720 coccidioidomycosis 9.4
1721 urethral intrinsic sphincter deficiency 9.4
1722 balanitis xerotica obliterans 9.4
1723 paranasal sinus disease 9.4
1724 hypermobility syndrome 9.4
1725 hypolipoproteinemia 9.4
1726 schistosomiasis 9.4
1727 plasmodium falciparum malaria 9.4
1728 anus cancer 9.4
1729 frozen shoulder 9.4
1730 pulmonary valve insufficiency 9.4
1731 noonan syndrome with multiple lentigines 9.4
1732 pleuropneumonia 9.4
1733 critical illness polyneuropathy 9.4
1734 autosomal dominant cerebellar ataxia 9.4
1735 glossopharyngeal neuralgia 9.4
1736 root resorption 9.4
1737 foster-kennedy syndrome 9.4
1738 hereditary angioedema 9.4
1739 aggressive periodontitis 9.4
1740 lymphangioma 9.4
1741 cystic echinococcosis 9.4
1742 echinococcosis 9.4
1743 dermatomycosis 9.4
1744 thrombocytopenia due to platelet alloimmunization 9.4
1745 lymphadenitis 9.4
1746 benign breast phyllodes tumor 9.4
1747 ichthyosis 9.4
1748 retinal vein occlusion 9.4
1749 histoplasmosis 9.4
1750 factitious disorder 9.4
1751 islet cell tumor 9.4
1752 neuroendocrine carcinoma 9.4
1753 neuritis 9.4
1754 childhood absence epilepsy 9.4
1755 atrial heart septal defect 9.4
1756 gaucher's disease 9.4
1757 hepatitis d 9.4
1758 heel spur 9.4
1759 ectodermal dysplasia 9.4
1760 tularemia 9.4
1761 brain germinoma 9.4
1762 vaginitis 9.4
1763 essential thrombocythemia 9.4
1764 focal epilepsy 9.4
1765 granulomatous hepatitis 9.4
1766 pharyngitis 9.4
1767 leptospirosis 9.4
1768 motor neuron disease 9.4
1769 generalized atherosclerosis 9.4
1770 macrocytic anemia 9.4
1771 relapsing-remitting multiple sclerosis 9.4
1772 glomus tumor 9.4
1773 hyperpituitarism 9.4
1774 central retinal vein occlusion 9.4
1775 protein s deficiency 9.4
1776 motor peripheral neuropathy 9.4
1777 enamel erosion 9.4
1778 splenic abscess 9.4
1779 opiate dependence 9.4
1780 agammaglobulinemia 9.4
1781 adenomyoma 9.4
1782 leydig cell tumor 9.4
1783 hemangioma of liver 9.4
1784 skin atrophy 9.4
1785 auditory system disease 9.4
1786 acalculous cholecystitis 9.4
1787 bruxism 9.4
1788 laryngeal squamous cell carcinoma 9.4
1789 cryoglobulinemia 9.4
1790 membranoproliferative glomerulonephritis 9.4
1791 testicular cancer 9.4
1792 acinar cell carcinoma 9.4
1793 mucinous adenocarcinoma 9.4
1794 thoracic outlet syndrome 9.4
1795 gastrointestinal system cancer 9.4
1796 mucinoses 9.4
1797 complex regional pain syndrome 9.4
1798 central nervous system lymphoma 9.4
1799 ovarian cystadenoma 9.4
1800 central nervous system disease 9.4
1801 osteitis fibrosa 9.4
1802 glycoproteinosis 9.4
1803 cranial nerve neoplasm 9.4
1804 cerebritis 9.4
1805 superior mesenteric artery syndrome 9.4
1806 appendix adenocarcinoma 9.4
1807 cervical adenocarcinoma 9.4
1808 cervical squamous cell carcinoma 9.4
1809 protein c deficiency 9.4
1810 vaginal discharge 9.4
1811 granuloma annulare 9.4
1812 posterior cerebral artery infarction 9.4
1813 colonic pseudo-obstruction 9.4
1814 vulvitis 9.4
1815 pituitary-dependent cushing's disease 9.4
1816 adrenal cortical adenocarcinoma 9.4
1817 thyroid gland medullary carcinoma 9.4
1818 bladder urothelial carcinoma 9.4
1819 linitis plastica 9.4
1820 mouth disease 9.4
1821 erythrasma 9.4
1822 biliary dyskinesia 9.4
1823 syphilis 9.4
1824 rh isoimmunization 9.4
1825 systemic scleroderma 9.4
1826 mutism 9.4
1827 microsporidiosis 9.4
1828 polyradiculoneuropathy 9.4
1829 myofascial pain syndrome 9.4
1830 granulomatous dermatitis 9.4
1831 somatostatinoma 9.4
1832 central nervous system germinoma 9.4
1833 pseudohypoaldosteronism 9.4
1834 myotonic disease 9.4
1835 bile duct cancer 9.4
1836 ulnar neuropathy 9.4
1837 somatoform disorder 9.4
1838 placenta accreta 9.4
1839 vasculogenic impotence 9.4
1840 proliferative glomerulonephritis 9.4
1841 diffuse glomerulonephritis 9.4
1842 immune-complex glomerulonephritis 9.4
1843 trachea carcinoma 9.4
1844 gastroesophageal junction adenocarcinoma 9.4
1845 alcoholic pancreatitis 9.4
1846 optic nerve glioma 9.4
1847 ganglioglioma 9.4
1848 middle ear disease 9.4
1849 aortic disease 9.4
1850 anterograde amnesia 9.4
1851 pulmonary coin lesion 9.4
1852 functioning pituitary adenoma 9.4
1853 t-cell acute lymphoblastic leukemia 9.4
1854 retinal disease 9.4
1855 well-differentiated liposarcoma 9.4
1856 gastric liposarcoma 9.4
1857 median neuropathy 9.4
1858 pyosalpinx 9.4
1859 adult lymphoma 9.4
1860 silent myocardial infarction 9.4
1861 esophageal disease 9.4
1862 mitral valve disease 9.4
1863 cll/sll 9.4
1864 central pontine myelinolysis 9.4
1865 acral lentiginous melanoma 9.4
1866 double outlet right ventricle 9.4
1867 pulmonary valve stenosis 9.4
1868 bilateral breast cancer 9.4
1869 hepatoblastoma 9.4
1870 skin tag 9.4
1871 mitochondrial metabolism disease 9.4
1872 anal canal squamous cell carcinoma 9.4
1873 axonal neuropathy 9.4
1874 peptic ulcer perforation 9.4
1875 parathyroid adenoma 9.4
1876 cocaine abuse 9.4
1877 chronic rhinitis 9.4
1878 scabies 9.4
1879 osteochondritis dissecans 9.4
1880 cyclothymic disorder 9.4
1881 actinomycosis 9.4
1882 mucormycosis 9.4
1883 acute cor pulmonale 9.4
1884 monocytic leukemia 9.4
1885 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.4
1886 malignant hyperthermia 9.4
1887 pyoderma gangrenosum 9.4
1888 oropharynx cancer 9.4
1889 herpes simplex 9.4
1890 nervous system disease 9.4
1891 gastroduodenitis 9.4
1892 vein disease 9.4
1893 leukoplakia of penis 9.4
1894 actinic keratosis 9.4
1895 neuromyelitis optica 9.4
1896 severe nonproliferative diabetic retinopathy 9.4
1897 hepatopulmonary syndrome 9.4
1898 visceral leishmaniasis 9.4
1899 speech disorder 9.4
1900 urea cycle disorder 9.4
1901 primary cerebellar degeneration 9.4
1902 viral infectious disease 9.4
1903 keratoconjunctivitis 9.4
1904 iridocyclitis 9.4
1905 blepharitis 9.4
1906 dextrocardia 9.4
1907 krukenberg carcinoma 9.4
1908 senile cataract 9.4
1909 cervical incompetence 9.4
1910 tenosynovitis 9.4
1911 refractive error 9.4
1912 accommodative esotropia 9.4
1913 esotropia 9.4
1914 alopecia areata 9.4
1915 lymph node disease 9.4
1916 hypoplastic left heart syndrome 9.4
1917 cocaine dependence 9.4
1918 factor v leiden thrombophilia 9.4
1919 keloid disorder 9.4
1920 limb-girdle muscular dystrophy 9.4
1921 alk-related neuroblastic tumor susceptibility 9.4
1922 berardinelli-seip congenital lipodystrophy 9.4
1923 chd2-related neurodevelopmental disorders 9.4
1924 cytochrome p450 oxidoreductase deficiency 9.4
1925 diabetes mellitus, 6q24-related transient neonatal 9.4
1926 heritable pulmonary arterial hypertension 9.4
1927 mbd5 haploinsufficiency 9.4
1928 prss1-related hereditary pancreatitis 9.4
1929 prothrombin-related thrombophilia 9.4
1930 rab18 deficiency 9.4
1931 trichorhinophalangeal syndrome 9.4
1932 amaurosis fugax 9.4
1933 aminoaciduria 9.4
1934 autoimmune atrophic gastritis 9.4
1935 autoimmune enteropathy 9.4
1936 autoimmune myocarditis 9.4
1937 binswanger's disease 9.4
1938 brittle diabetes 9.4
1939 broken heart syndrome 9.4
1940 cataract-glaucoma 9.4
1941 central congenital hypothyroidism 9.4
1942 chromosome 16q duplication 9.4
1943 chromosome 19q duplication 9.4
1944 chromosome 4p deletion 9.4
1945 chromosome 5p duplication 9.4
1946 chronic thromboembolic pulmonary hypertension 9.4
1947 coccygodynia 9.4
1948 congenital hydrocephalus 9.4
1949 congenitally corrected transposition of the great arteries 9.4
1950 coronary artery aneurysm 9.4
1951 diencephalic syndrome 9.4
1952 distal renal tubular acidosis 9.4
1953 dock2 deficiency 9.4
1954 double discordia 9.4
1955 elective mutism 9.4
1956 familial colorectal cancer 9.4
1957 gas bloat syndrome 9.4
1958 hemophilic arthropathy 9.4
1959 hemorrhagic proctocolitis 9.4
1960 hemorrhagic shock and encephalopathy syndrome 9.4
1961 homologous wasting disease 9.4
1962 horseshoe kidney 9.4
1963 idiopathic hypersomnia 9.4
1964 insulin-resistance type b 9.4
1965 itch e3 ubiquitin ligase deficiency 9.4
1966 jackhammer esophagus 9.4
1967 kikuchi disease 9.4
1968 klebsiella infection 9.4
1969 lymphangiectasis 9.4
1970 lymphosarcoma 9.4
1971 myoclonus epilepsy 9.4
1972 neonatal meningitis 9.4
1973 neuroendocrine carcinoma of the cervix 9.4
1974 oral cancer 9.4
1975 pachygyria 9.4
1976 pancreatitis, pediatric 9.4
1977 papular mucinosis 9.4
1978 plasmablastic lymphoma 9.4
1979 post-traumatic epilepsy 9.4
1980 primary central nervous system lymphoma 9.4
1981 progressive transformation of germinal centers 9.4
1982 pseudo-turner syndrome 9.4
1983 retinochoroidal coloboma 9.4
1984 ring chromosome 13 9.4
1985 secondary adrenal insufficiency 9.4
1986 skeletal dysplasias 9.4
1987 sudden arrhythmia death syndrome 9.4
1988 supraglottic laryngeal cancer 9.4
1989 thyrotoxic periodic paralysis 9.4
1990 trochlear dysplasia 9.4
1991 uniparental disomy of chromosome 2 9.4
1992 uterine sarcoma 9.4
1993 age-related hearing loss 9.4
1994 atrial fibrillation and stroke 9.4
1995 central cord syndrome 9.4
1996 cerebral arteriosclerosis 9.4
1997 cumulative trauma disorders 9.4
1998 hemifacial spasm 9.4
1999 myoclonus 9.4
2000 overuse syndrome 9.4
2001 repetitive motion disorders 9.4
2002 spasticity 9.4
2003 audiogenic seizures 9.4
2004 cleft lip with or without cleft palate 9.4
2005 primary peritoneal carcinoma 9.4
2006 mixed germ cell tumor 9.4
2007 genetic neuromuscular disease 9.4
2008 systemic autoimmune disease 9.4
2009 adrenogenital syndrome 9.4
2010 immune complex mediated vasculitis 9.4
2011 low-grade astrocytoma 9.4
2012 papillary tumor of the pineal region 9.4
2013 uniparental disomy of chromosome 14 9.4
2014 rare lymphatic malformation 9.4
2015 cerebral sinovenous thrombosis 9.4
2016 lmna-related cardiocutaneous progeria syndrome 9.4
2017 idiopathic nephrotic syndrome 9.4
2018 congenital pseudoarthrosis of the tibia 9.4
2019 familial intrahepatic cholestasis 9.4
2020 acyl-coa dehydrogenase deficiency 9.4
2021 homozygous familial hypercholesterolemia 9.4
2022 idiopathic avascular necrosis 9.4
2023 osteonecrosis of the jaw 9.4
2024 spontaneous intracranial hypotension 9.4
2025 primitive portal vein thrombosis 9.4
2026 secondary sclerosing cholangitis 9.4
2027 semicircular canal dehiscence syndrome 9.4
2028 idiopathic gastroparesis 9.4
2029 pattern dystrophy 9.4
2030 argyria 9.4
2031 disorder of energy metabolism 9.4
2032 disorder of purine metabolism 9.4
2033 resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha 9.4
2034 rare intellectual disability 9.4
2035 primary lipodystrophy 9.4
2036 other metabolic disease 9.4
2037 non-functioning pituitary adenoma 9.4
2038 microtia 9.4
2039 lumbar syndrome 9.4
2040 autosomal trisomy 9.4
2041 paternal uniparental disomy 9.4
2042 polyploidy 9.4
2043 severe immune-mediated enteropathy 9.4
2044 x-linked emery-dreifuss muscular dystrophy 9.4
2045 acute motor axonal neuropathy 9.4
2046 multiple system atrophy, parkinsonian type 9.4
2047 colobomatous microphthalmia 9.4
2048 acquired lipodystrophy 9.4
2049 intestinal polyposis syndrome 9.4
2050 undetermined colitis 9.4
2051 multiple congenital anomalies/dysmorphic syndrome-intellectual disability 9.4
2052 polyendocrinopathy 9.4
2053 neurogenic thoracic outlet syndrome 9.4
2054 cutaneous myiasis 9.4
2055 precursor t-cell acute lymphoblastic leukemia 9.4

Graphical network of the top 20 diseases related to Body Mass Index Quantitative Trait Locus 12:



Diseases related to Body Mass Index Quantitative Trait Locus 12

Symptoms & Phenotypes for Body Mass Index Quantitative Trait Locus 12

Clinical features from OMIM:

612362

UMLS symptoms related to Body Mass Index Quantitative Trait Locus 12:


symptoms, high weight, obesity, metabolically benign, monogenic obesity

Drugs & Therapeutics for Body Mass Index Quantitative Trait Locus 12

Drugs for Body Mass Index Quantitative Trait Locus 12 (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(showing 1120, show less)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1
Citalopram Approved Phase 4 59729-33-8 2771
2
Oseltamivir Approved Phase 4 204255-11-8, 196618-13-0 65028
3
Enalapril Approved, Vet_approved Phase 4 75847-73-3 40466924 5362032
4
Enalaprilat Approved Phase 4 76420-72-9 6917719
5
Lactitol Approved, Investigational Phase 4 585-88-6, 585-86-4 493591
6
Clonidine Approved Phase 4 4205-90-7 2803
7
Erythromycin Approved, Investigational, Vet_approved Phase 4 114-07-8 12560 441411
8
Clopidogrel Approved Phase 4 113665-84-2, 120202-66-6 60606
9
Metyrapone Approved, Investigational Phase 4 54-36-4 4174
10
Norfloxacin Approved Phase 4 70458-96-7 4539