BMIQ12
MCID: BDY015
MIFTS: 48

Body Mass Index Quantitative Trait Locus 12 (BMIQ12)

Categories: Bone diseases, Endocrine diseases, Genetic diseases, Metabolic diseases, Rare 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 57 29 6 40
Obesity, Susceptibility to, Bmiq12 57 13
Obesity 57 72
Obesity, Susceptibility to 57
Obesity Bmiq12 57
Bmiq12 57

Classifications:



External Ids:

OMIM 57 612362
UMLS 72 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 proprotein convertase 1/3 deficiency and body mass index quantitative trait locus 11, 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 Oseltamivir and Citalopram 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 2059, show less)
# Related Disease Score Top Affiliating Genes
1 proprotein convertase 1/3 deficiency 32.0 PCSK1 LOC101929710
2 body mass index quantitative trait locus 11 12.8
3 obesity, early-onset, with adrenal insufficiency and red hair 12.7
4 morbid obesity and spermatogenic failure 12.6
5 obesity-hypoventilation syndrome 12.6
6 genetic obesity 12.5
7 mental retardation, truncal obesity, retinal dystrophy, and micropenis syndrome 12.5
8 obesity, hyperphagia, and developmental delay 12.5
9 abdominal obesity-metabolic syndrome 1 12.5
10 spastic paraplegia, intellectual disability, nystagmus, and obesity 12.5
11 retinal dystrophy and obesity 12.5
12 leptin deficiency or dysfunction 12.5
13 obesity due to congenital leptin deficiency 12.5
14 abdominal obesity-metabolic syndrome 3 12.5
15 wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome 12.5
16 developmental delay, intellectual disability, obesity, and dysmorphism 12.5
17 hypothalamic obesity 12.4
18 hydrocephalus obesity hypogonadism 12.4
19 x-linked intellectual disability - short stature - obesity 12.4
20 body mass index quantitative trait locus 19 12.4
21 leptin receptor deficiency 12.3
22 body mass index quantitative trait locus 20 12.3
23 abdominal obesity-metabolic syndrome quantitative trait locus 2 12.3
24 aniridia - ptosis - intellectual disability - familial obesity 12.3
25 intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity 12.3
26 rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome 12.2
27 coloboma-obesity-hypogenitalism-mental retardation syndrome 12.2
28 short stature-obesity syndrome 12.2
29 mental retardation, obesity, mandibular prognathism, and eye and skin anomalies 12.2
30 prolactin deficiency with obesity and enlarged testes 12.2
31 obesity due to congenital leptin resistance 12.2
32 severe early-onset obesity-insulin resistance syndrome due to sh2b1 deficiency 12.2
33 obesity due to sim1 deficiency 12.2
34 wilson-turner x-linked mental retardation syndrome 12.2
35 syndromic obesity 12.2
36 body mass index quantitative trait locus 9 12.2
37 body mass index quantitative trait locus 4 12.2
38 cohen syndrome 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 midface hypoplasia, obesity, developmental delay, and neonatal hypotonia 12.2
44 body mass index quantitative trait locus 10 12.1
45 mehmo syndrome 12.1
46 genetic non-syndromic obesity 12.1
47 momo syndrome 12.1
48 chops syndrome 12.1
49 congenital leptin deficiency 12.0
50 genetic overgrowth/obesity syndrome 12.0
51 overgrowth/obesity syndrome 12.0
52 x-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome 12.0
53 intellectual disability-seizures-macrocephaly-obesity syndrome 12.0
54 intellectual disability-obesity-brain malformations-facial dysmorphism syndrome 12.0
55 obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome 12.0
56 obsolete: x-linked intellectual disability-precocious puberty-obesity syndrome 12.0
57 obsolete: x-linked intellectual disability-obesity-short stature syndrome 12.0
58 obesity, hyperphagia, and severe developmental delay due totrkb gene deficiency 12.0
59 ayazi syndrome 11.9
60 rohhad 11.9
61 coenzyme q10 deficiency, primary, 2 11.8
62 hyperostosis frontalis interna 11.8
63 fatty liver disease 11.7
64 polycystic ovary syndrome 11.7
65 prader-willi syndrome 11.7
66 man1b1-cdg 11.7
67 diabetes mellitus, noninsulin-dependent 11.7
68 non-alcoholic fatty liver disease 11.6
69 alstrom syndrome 11.6
70 bardet-biedl syndrome 11.6
71 carpenter syndrome 1 11.6
72 glucose intolerance 11.6
73 bardet-biedl syndrome 1 11.6
74 sleep apnea 11.6
75 diploid-triploid mosaicism 11.6
76 pseudohypoparathyroidism, type ia 11.6
77 borjeson-forssman-lehmann syndrome 11.6
78 fatty liver disease, nonalcoholic 1 11.5
79 eating disorder 11.5
80 chromosome 16p11.2 deletion syndrome, 220-kb 11.5
81 bardet-biedl syndrome 3 11.5
82 mental retardation, autosomal dominant 39 11.5
83 conn's syndrome 11.5
84 gestational diabetes 11.5
85 hypertriglyceridemia, familial 11.5
86 gallbladder disease 1 11.5
87 bardet-biedl syndrome 4 11.5
88 bardet-biedl syndrome 2 11.5
89 pseudopseudohypoparathyroidism 11.5
90 adiposis dolorosa 11.5
91 laron syndrome 11.5
92 non-alcoholic steatohepatitis 11.4
93 pre-eclampsia 11.4
94 vascular disease 11.4
95 diabetes mellitus, ketosis-prone 11.4
96 prediabetes syndrome 11.4
97 bardet-biedl syndrome 6 11.4
98 wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 11.4
99 pituitary adenoma 4, acth-secreting 11.4
100 acanthosis nigricans 11.4
101 achondroplasia 11.4
102 hyperlipoproteinemia, type iii 11.4
103 bardet-biedl syndrome 5 11.4
104 bardet-biedl syndrome 9 11.4
105 pulmonary embolism 11.4
106 bardet-biedl syndrome 7 11.4
107 breast cancer 11.4
108 aromatase deficiency 11.4
109 bardet-biedl syndrome 8 11.4
110 bardet-biedl syndrome 10 11.4
111 bardet-biedl syndrome 14 11.4
112 bardet-biedl syndrome 21 11.4
113 kleefstra syndrome 11.4
114 clark-baraitser syndrome 11.3
115 camera-marugo-cohen syndrome 11.3
116 biemond syndrome ii 11.3
117 hepatocellular carcinoma 11.3
118 hernia, hiatus 11.3
119 migraine with or without aura 1 11.3
120 gout 11.3
121 neural tube defects 11.3
122 renal cell carcinoma, nonpapillary 11.3
123 focal segmental glomerulosclerosis 11.3
124 stroke, ischemic 11.3
125 varicose veins 11.3
126 myeloma, multiple 11.3
127 esophageal cancer 11.3
128 body mass index quantitative trait locus 1 11.3
129 mckusick-kaufman syndrome 11.3
130 hypersomnia 11.3
131 adiponectin, serum level of, quantitative trait locus 1 11.2
132 blount's disease 11.2
133 acth-secreting pituitary adenoma 11.2
134 pseudohypoparathyroidism with albright hereditary osteodystrophy 11.2
135 smith-magenis syndrome 11.2
136 empty sella syndrome 11.2
137 polycystic ovary syndrome 1 11.2
138 monogenic diabetes 11.2
139 alopecia, androgenetic, 1 11.2
140 lipodystrophy, familial partial, type 2 11.2
141 chromosome 16p13.3 deletion syndrome, proximal 11.2
142 schaaf-yang syndrome 11.2
143 idiopathic edema 11.2
144 primary pigmented nodular adrenocortical disease 11.2
145 rickets 11.2
146 maturity-onset diabetes of the young, type 2 11.2
147 mental retardation, x-linked, syndromic, cabezas type 11.2
148 neutral lipid storage disease with myopathy 11.2
149 syndromic x-linked intellectual disability 7 11.2
150 bell's palsy 11.2
151 carcinosarcoma 11.2
152 froelich syndrome 11.2
153 biemond syndrome 11.2
154 classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 11.2
155 hyperadrenalism 11.2
156 bardet-biedl syndrome 12 11.2
157 ulnar-mammary syndrome 11.1
158 pseudohypoparathyroidism, type ic 11.1
159 lipid metabolism disorder 11.1
160 hyperinsulinism 11.1
161 acrodysostosis 1 with or without hormone resistance 11.0
162 chromosome 16p12.1 deletion syndrome, 520-kb 11.0
163 growth hormone insensitivity with immunodeficiency 11.0
164 prader-willi habitus, osteopenia, and camptodactyly 11.0
165 chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb 11.0
166 carpenter syndrome 2 11.0
167 pigmented nodular adrenocortical disease, primary, 4 11.0
168 bardet-biedl syndrome 11 11.0
169 bardet-biedl syndrome 13 11.0
170 bardet-biedl syndrome 16 11.0
171 bardet-biedl syndrome 17 11.0
172 bardet-biedl syndrome 18 11.0
173 bardet-biedl syndrome 19 11.0
174 bardet-biedl syndrome 20 11.0
175 cortisone reductase deficiency 11.0
176 pelvic lipomatosis 11.0
177 2q37 deletion syndrome 11.0
178 short stature, brachydactyly, intellectual developmental disability, and seizures 11.0
179 hyperglycemia 11.0
180 liver disease 10.9
181 diabetes mellitus 10.9
182 pituitary adenoma 1, multiple types 10.9
183 hepatitis b vaccine, response to 10.9
184 precocious puberty, central, 1 10.9
185 cerebrooculofacioskeletal syndrome 1 10.9
186 acth-independent macronodular adrenal hyperplasia 10.9
187 mental retardation, x-linked, syndromic, nascimento type 10.9
188 chromosome xq27.3-q28 duplication syndrome 10.9
189 diabetes mellitus, noninsulin-dependent, 1 10.9
190 renal cell carcinoma, papillary, 1 10.9
191 high density lipoprotein cholesterol level quantitative trait locus 1 10.9
192 coronary artery disease, autosomal dominant, 1 10.9
193 lipodystrophy, familial partial, type 1 10.9
194 pigmented nodular adrenocortical disease, primary, 2 10.9
195 pigmented nodular adrenocortical disease, primary, 1 10.9
196 diabetes mellitus, insulin-resistant, with acanthosis nigricans 10.9
197 chromosome 3q29 duplication syndrome 10.9
198 pigmented nodular adrenocortical disease, primary, 3 10.9
199 precocious puberty, central, 2 10.9
200 acth-independent macronodular adrenal hyperplasia 2 10.9
201 bardet-biedl syndrome 15 10.9
202 diabetes mellitus, noninsulin-dependent, 5 10.9
203 temple syndrome 10.9
204 white-sutton syndrome 10.9
205 senior-loken syndrome 9 10.9
206 luscan-lumish syndrome 10.9
207 chromosome 15q24 deletion syndrome 10.9
208 syndromic x-linked intellectual disability shashi type 10.9
209 16p11.2 deletion syndrome 10.9
210 48,xxyy syndrome 10.9
211 adnp syndrome 10.9
212 cerebro-oculo-facio-skeletal syndrome 10.9
213 cockayne syndrome type ii 10.9
214 hernández-aguirre negrete syndrome 10.9
215 lipodermatosclerosis 10.9
216 localized lipodystrophy 10.9
217 macular telangiectasia type 2 10.9
218 male pseudohermaphroditism intellectual disability syndrome, verloes type 10.9
219 mthfr gene variant 10.9
220 proximal chromosome 18q deletion syndrome 10.9
221 septo-optic dysplasia spectrum 10.9
222 coronary heart disease 1 10.8
223 hypercholesterolemia, familial, 1 10.8
224 osteoarthritis 10.7
225 gastroesophageal reflux 10.7
226 chronic kidney disease 10.7
227 atherosclerosis susceptibility 10.7
228 kidney disease 10.7
229 heart disease 10.7
230 endometrial cancer 10.7
231 hypoglycemia 10.7
232 asthma 10.7
233 lipedema 10.6
234 congestive heart failure 10.6
235 hypogonadism 10.6
236 hypogonadotropism 10.6
237 hyperandrogenism 10.6
238 apnea, obstructive sleep 10.6
239 hypertension, essential 10.6
240 infertility 10.6
241 overnutrition 10.6
242 colorectal cancer 10.6
243 hypothyroidism 10.6
244 anorexia nervosa 10.6
245 depression 10.6
246 coronary artery anomaly 10.6
247 hypervitaminosis d 10.6
248 hyperuricemia 10.6
249 arteries, anomalies of 10.6
250 end stage renal failure 10.6
251 periodontitis 10.6
252 insulin-like growth factor i 10.6
253 respiratory failure 10.5
254 sleep disorder 10.5
255 placenta disease 10.5
256 autoimmune disease 10.5
257 rapidly involuting congenital hemangioma 10.5
258 anxiety 10.5
259 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.5
260 impotence 10.5
261 proteasome-associated autoinflammatory syndrome 1 10.5
262 attention deficit-hyperactivity disorder 10.5
263 pustulosis of palm and sole 10.5
264 psoriasis 10.5
265 atrial fibrillation 10.5
266 esophagitis 10.5
267 thyroiditis 10.5
268 iron metabolism disease 10.5
269 hair whorl 10.5
270 eclampsia 10.5
271 cytokine deficiency 10.5
272 microvascular complications of diabetes 3 10.5
273 microvascular complications of diabetes 4 10.5
274 microvascular complications of diabetes 6 10.5
275 microvascular complications of diabetes 7 10.5
276 mental depression 10.5
277 mood disorder 10.5
278 liver cirrhosis 10.5
279 osteoporosis 10.5
280 bulimia nervosa 10.5
281 bone mineral density quantitative trait locus 8 10.5
282 bone mineral density quantitative trait locus 15 10.5
283 back pain 10.4
284 prostate cancer 10.4
285 dental caries 10.4
286 major depressive disorder 10.4
287 cholelithiasis 10.4
288 cerebrovascular disease 10.4
289 diabetes mellitus, insulin-dependent 10.4
290 severe combined immunodeficiency 10.4
291 pancreatic cancer 10.4
292 acute pancreatitis 10.4
293 aging 10.4
294 alacrima, achalasia, and mental retardation syndrome 10.4
295 anovulation 10.4
296 overgrowth syndrome 10.4
297 hashimoto thyroiditis 10.4
298 pulmonary disease, chronic obstructive 10.4
299 resting heart rate, variation in 10.4
300 adenoma 10.4
301 pulmonary hypertension 10.4
302 constipation 10.4
303 acute insulin response 10.4
304 hyperparathyroidism 10.4
305 thrombophilia due to thrombin defect 10.4
306 neuropathy 10.4
307 gallbladder disease 10.4
308 bipolar disorder 10.4
309 48,xyyy 10.4
310 47,xyy 10.4
311 hypoxia 10.4
312 major affective disorder 8 10.4
313 major affective disorder 9 10.4
314 arteriosclerosis 10.4
315 adenocarcinoma 10.4
316 inflammatory bowel disease 10.4
317 atrial standstill 1 10.4
318 kidney cancer 10.4
319 peripheral vascular disease 10.4
320 bone resorption disease 10.4
321 lung disease 10.4
322 autonomic dysfunction 10.4
323 myocardial infarction 10.4
324 craniopharyngioma 10.4
325 barrett esophagus 10.4
326 ischemia 10.4
327 chronic pain 10.4
328 huntington disease-like 2 10.4
329 sexual disorder 10.4
330 lymphocytic leukemia 10.4
331 intracranial hypertension 10.4
332 fetal macrosomia 10.4
333 alcohol dependence 10.4
334 nephrolithiasis, calcium oxalate 10.4
335 pain agnosia 10.4
336 ige responsiveness, atopic 10.4
337 lymphedema 10.4
338 diarrhea 10.3
339 ventral hernia 10.3
340 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.3
341 leukemia, acute lymphoblastic 10.3
342 autism 10.3
343 alcohol use disorder 10.3
344 pancreatitis 10.3
345 down syndrome 10.3
346 secondary hyperparathyroidism 10.3
347 gastritis 10.3
348 nutritional deficiency disease 10.3
349 headache 10.3
350 alzheimer disease 10.3
351 rectum cancer 10.3
352 autism spectrum disorder 10.3
353 disease of mental health 10.3
354 dysphagia 10.3
355 acute respiratory distress syndrome 10.3
356 cardiac conduction defect 10.3
357 periodontitis, chronic 10.3
358 microvascular complications of diabetes 5 10.3
359 thrombosis 10.3
360 hypogonadotropic hypogonadism 10.3
361 cholecystitis 10.3
362 fibrosis of extraocular muscles, congenital, 1 10.3
363 peripheral nervous system disease 10.3
364 acute myocardial infarction 10.3
365 personality disorder 10.3
366 appendicitis 10.3
367 amenorrhea 10.3
368 rhinitis 10.3
369 hypotonia 10.3
370 spinal cord injury 10.3
371 ovarian cancer 10.3
372 deficiency anemia 10.3
373 prostatic hypertrophy 10.3
374 acute cystitis 10.3
375 rheumatoid arthritis 10.3
376 male infertility 10.3
377 substance abuse 10.3
378 dementia 10.3
379 gastric cancer 10.3
380 cardiac arrest 10.3
381 acute kidney failure 10.3
382 thyroid carcinoma 10.3
383 neurofibromatosis, type ii 10.2
384 intracranial hypertension, idiopathic 10.2
385 prostatic adenoma 10.2
386 prostatic hyperplasia, benign 10.2
387 allergic rhinitis 10.2
388 colorectal adenoma 10.2
389 ovarian disease 10.2
390 schizophrenia 10.2
391 pik3ca-related overgrowth syndrome 10.2
392 huntington disease-like 3 10.2
393 hypopituitarism 10.2
394 growth hormone deficiency 10.2
395 dermatitis, atopic 10.2
396 toxic shock syndrome 10.2
397 skin disease 10.2
398 insulinoma 10.2
399 alexithymia 10.2
400 peritonitis 10.2
401 pulmonary alveolar microlithiasis 10.2
402 peptic esophagitis 10.2
403 dermatitis 10.2
404 lipomatosis 10.2
405 arthritis 10.2
406 encephalopathy 10.2
407 hypervitaminosis a 10.2
408 carotenemia 10.2
409 pelvic organ prolapse 10.2
410 bone disease 10.2
411 dumping syndrome 10.2
412 fibromyalgia 10.2
413 yemenite deaf-blind hypopigmentation syndrome 10.2
414 psoriatic arthritis 10.2
415 dyspepsia 10.2
416 hyperthyroidism 10.2
417 precocious puberty 10.2
418 cervical cancer 10.2
419 venous insufficiency 10.2
420 avoidant personality disorder 10.2
421 viral hepatitis 10.2
422 cellulitis 10.2
423 crohn's disease 10.2
424 helicobacter pylori infection 10.2
425 homocysteinemia 10.2
426 irritable bowel syndrome 10.2
427 bladder cancer 10.2
428 angina pectoris 10.2
429 nephrotic syndrome 10.2
430 hepatitis c 10.2
431 aortic aneurysm 10.2
432 peptic ulcer disease 10.2
433 muscular atrophy 10.2
434 ileus 10.2
435 hyperprolactinemia 10.2
436 low compliance bladder 10.2
437 celiac disease 1 10.2
438 colitis 10.2
439 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 10.2
440 muscle hypertrophy 10.2
441 hydrops, lactic acidosis, and sideroblastic anemia 10.2
442 autonomic neuropathy 10.2
443 cerebral palsy 10.2
444 arthropathy 10.2
445 ulcerative colitis 10.2
446 aortic aneurysm, familial abdominal, 1 10.1
447 multiple sclerosis 10.1
448 triiodothyronine receptor auxiliary protein 10.1
449 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 10.1
450 gastrojejunal ulcer 10.1
451 iron deficiency anemia 10.1
452 bronchitis 10.1
453 influenza 10.1
454 aneurysm 10.1
455 intussusception 10.1
456 endometrial hyperplasia 10.1
457 allergic hypersensitivity disease 10.1
458 hemosiderosis 10.1
459 schizoaffective disorder 10.1
460 b-cell lymphoma 10.1
461 diverticulitis 10.1
462 cataract 10.1
463 learning disability 10.1
464 allergic asthma 10.1
465 systolic heart failure 10.1
466 goiter 10.1
467 polyneuropathy 10.1
468 metabolic acidosis 10.1
469 renal fibrosis 10.1
470 gastric ulcer 10.1
471 wernicke encephalopathy 10.1
472 pneumonia 10.1
473 narcolepsy 10.1
474 lung cancer 10.1
475 immunodeficiency, common variable, 10 10.1
476 pulmonary edema 10.1
477 systemic lupus erythematosus 10.1
478 pulmonary hypertension, primary, 1 10.1
479 lymphoma, hodgkin, classic 10.1
480 creatinine clearance quantitative trait locus 10.1
481 lymphoma 10.1
482 keratosis 10.1
483 gingivitis 10.1
484 heart valve disease 10.1
485 paraplegia 10.1
486 ovarian epithelial cancer 10.1
487 rare hereditary hemochromatosis 10.1
488 polydactyly 10.1
489 ectodermal dysplasia-syndactyly syndrome 2 10.1
490 vitamin b12 deficiency 10.1
491 childhood acute lymphocytic leukemia 10.1
492 familial hyperlipidemia 10.1
493 neutropenia 10.1
494 dilated cardiomyopathy 10.1
495 rheumatic disease 10.1
496 compartment syndrome 10.1
497 polycythemia 10.1
498 achalasia 10.1
499 hypogonadism, male 10.1
500 arts syndrome 10.1
501 lymphoma, non-hodgkin, familial 10.1
502 bone mineral density quantitative trait locus 3 10.1
503 hepatitis b 10.1
504 coronary stenosis 10.1
505 postpartum depression 10.1
506 dwarfism 10.1
507 slipped capital femoral epiphysis 10.1
508 cryptogenic cirrhosis 10.1
509 carpal tunnel syndrome 10.1
510 ataxia and polyneuropathy, adult-onset 10.1
511 leukemia, acute myeloid 10.1
512 leukemia, acute lymphoblastic 3 10.1
513 helix syndrome 10.1
514 limb ischemia 10.1
515 physical disorder 10.1
516 hydrocephalus 10.1
517 leukemia 10.1
518 beriberi 10.1
519 lactic acidosis 10.1
520 pseudohypoparathyroidism 10.1
521 intestinal obstruction 10.1
522 intermediate coronary syndrome 10.1
523 lupus erythematosus 10.1
524 diabetes insipidus 10.1
525 congenital hydrocephalus 10.1
526 rare disease in surgical orthopedic 10.1
527 otitis media 10.1
528 infant gynecomastia 10.1
529 gynecomastia 10.1
530 duodenal ulcer 10.1
531 combined t cell and b cell immunodeficiency 10.1
532 situs inversus 10.1
533 hypereosinophilic syndrome 10.1
534 tobacco addiction 10.0
535 meningioma, radiation-induced 10.0
536 maturity-onset diabetes of the young 10.0
537 meningioma, familial 10.0
538 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.0
539 gastrointestinal ulceration, recurrent, with dysfunctional platelets 10.0
540 chorioamnionitis 10.0
541 autosomal recessive disease 10.0
542 scoliosis 10.0
543 endometritis 10.0
544 sialadenitis 10.0
545 spinal meningioma 10.0
546 melanoma 10.0
547 iga glomerulonephritis 10.0
548 hypokalemia 10.0
549 secretory meningioma 10.0
550 lymphoplasmacyte-rich meningioma 10.0
551 alopecia 10.0
552 ocular motor apraxia 10.0
553 thoracoabdominal syndrome 10.0
554 macular degeneration, age-related, 1 10.0
555 gastrointestinal stromal tumor 10.0
556 smoking as a quantitative trait locus 3 10.0
557 bacterial infectious disease 10.0
558 diphtheria 10.0
559 hypertensive heart disease 10.0
560 thrombocytopenia 10.0
561 enthesopathy 10.0
562 post-traumatic stress disorder 10.0
563 acromegaly 10.0
564 synovitis 10.0
565 pancreatic ductal adenocarcinoma 10.0
566 bladder disease 10.0
567 panic disorder 10.0
568 acute stress disorder 10.0
569 spinal stenosis 10.0
570 gastrointestinal system disease 10.0
571 myeloid leukemia 10.0
572 simpson-golabi-behmel syndrome 10.0
573 premature aging 10.0
574 hypercarotenemia and vitamin a deficiency, autosomal dominant 10.0
575 obsessive-compulsive disorder 10.0
576 diffuse large b-cell lymphoma 10.0
577 chronic venous insufficiency 10.0
578 osteomalacia 10.0
579 keratomalacia 10.0
580 gastroparesis 10.0
581 conduct disorder 10.0
582 familial hypercholesterolemia 10.0
583 thrombophilia 10.0
584 psychotic disorder 10.0
585 gallbladder cancer 10.0
586 glucose metabolism disease 10.0
587 retinal degeneration 10.0
588 vascular dementia 10.0
589 diastolic heart failure 10.0
590 drug dependence 10.0
591 seizure disorder 10.0
592 hyperlipidemia, familial combined, 3 10.0
593 retinitis pigmentosa 10.0
594 mend syndrome 10.0
595 global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 10.0
596 peripheral artery disease 10.0
597 steatorrhea 10.0
598 pyelonephritis 10.0
599 cholestasis 10.0
600 hidradenitis suppurativa 10.0
601 endometriosis 10.0
602 pancreatic adenocarcinoma 10.0
603 pituitary gland disease 10.0
604 fasciitis 10.0
605 diabetic neuropathy 10.0
606 hypertrophic cardiomyopathy 10.0
607 allergic encephalomyelitis 10.0
608 dextrocardia with situs inversus 10.0
609 brain injury 10.0
610 paresthesia 10.0
611 traumatic brain injury 10.0
612 ciliopathy 10.0
613 glomerular disease 10.0
614 cryptorchidism, unilateral or bilateral 10.0
615 hepatitis c virus 10.0
616 graft-versus-host disease 10.0
617 sensorineural hearing loss 10.0
618 chlamydia 10.0
619 inflammatory spondylopathy 10.0
620 candidiasis 10.0
621 hidradenitis 10.0
622 retinal vascular disease 10.0
623 pancreas disease 10.0
624 endometrial adenocarcinoma 10.0
625 skin carcinoma 10.0
626 intermittent claudication 10.0
627 prostate disease 10.0
628 scrapie 10.0
629 spondylitis 10.0
630 degenerative disc disease 10.0
631 muscular dystrophy 10.0
632 chromosomal triplication 10.0
633 dentinogenesis imperfecta type 2 10.0
634 head injury 10.0
635 retinoblastoma 10.0
636 hutterite cerebroosteonephrodysplasia syndrome 10.0
637 angiosarcoma 10.0
638 neuroretinitis 10.0
639 visual epilepsy 10.0
640 acute leukemia 10.0
641 papilledema 10.0
642 cholera 10.0
643 pneumothorax 10.0
644 bilirubin metabolic disorder 10.0
645 food allergy 10.0
646 retinitis 10.0
647 familial retinoblastoma 10.0
648 thyroid gland disease 10.0
649 lymphopenia 10.0
650 microcephaly 10.0
651 heparin-induced thrombocytopenia 10.0
652 spondyloarthropathy 1 9.9
653 pheochromocytoma 9.9
654 spondylolisthesis 9.9
655 arterial calcification, generalized, of infancy, 1 9.9
656 taqi polymorphism 9.9
657 fetal akinesia deformation sequence 2 9.9
658 tendinitis 9.9
659 exanthem 9.9
660 hepatocellular adenoma 9.9
661 adrenal gland pheochromocytoma 9.9
662 inguinal hernia 9.9
663 aortic atherosclerosis 9.9
664 renal hypertension 9.9
665 portal hypertension 9.9
666 pertussis 9.9
667 primary hyperparathyroidism 9.9
668 social phobia 9.9
669 nephrosclerosis 9.9
670 atypical depressive disorder 9.9
671 alcoholic hepatitis 9.9
672 autoimmune hepatitis 9.9
673 glomerulonephritis 9.9
674 pituitary adenoma 9.9
675 elephantiasis 9.9
676 eye disease 9.9
677 gastric cardia adenocarcinoma 9.9
678 amyloidosis 9.9
679 dyskinesia of esophagus 9.9
680 cholangitis 9.9
681 substance dependence 9.9
682 hypoalphalipoproteinemia 9.9
683 pituitary tumors 9.9
684 cardiogenic shock 9.9
685 cardiac arrhythmia 9.9
686 cleft palate, isolated 9.9
687 lipoid congenital adrenal hyperplasia 9.9
688 hemochromatosis, type 1 9.9
689 pancreatic agenesis 1 9.9
690 branchiootic syndrome 1 9.9
691 ovarian hyperstimulation syndrome 9.9
692 tendinopathy 9.9
693 aspiration pneumonia 9.9
694 restless legs syndrome 9.9
695 microinvasive gastric cancer 9.9
696 borderline personality disorder 9.9
697 hydronephrosis 9.9
698 dysthymic disorder 9.9
699 leiomyoma 9.9
700 quadriplegia 9.9
701 severe pre-eclampsia 9.9
702 bipolar i disorder 9.9
703 estrogen excess 9.9
704 panniculitis 9.9
705 epilepsy 9.9
706 hyperostosis 9.9
707 papilloma 9.9
708 thrombophlebitis 9.9
709 neuromuscular disease 9.9
710 clear cell renal cell carcinoma 9.9
711 uremia 9.9
712 ovarian cyst 9.9
713 intestinal volvulus 9.9
714 vasculitis 9.9
715 pathologic nystagmus 9.9
716 developmental coordination disorder 9.9
717 periodontal ehlers-danlos syndrome 9.9
718 central precocious puberty 9.9
719 developmental dyspraxia 9.9
720 syncope 9.9
721 tremor 9.9
722 rare surgical neurologic disease 9.9
723 sarcoidosis 1 9.9
724 anencephaly 9.9
725 cystic fibrosis 9.9
726 graves disease 1 9.9
727 wilms tumor 5 9.9
728 ventricular fibrillation, paroxysmal familial, 1 9.9
729 carotid intimal medial thickness 2 9.9
730 cyanosis, transient neonatal 9.9
731 aortic valve disease 2 9.9
732 chlamydia pneumonia 9.9
733 estrogen-receptor positive breast cancer 9.9
734 umbilical hernia 9.9
735 blind loop syndrome 9.9
736 protein-energy malnutrition 9.9
737 azoospermia 9.9
738 squamous cell carcinoma 9.9
739 hypothalamic disease 9.9
740 exostosis 9.9
741 hepatitis 9.9
742 purpura 9.9
743 plague 9.9
744 gastric adenocarcinoma 9.9
745 agoraphobia 9.9
746 mediastinitis 9.9
747 night blindness 9.9
748 cleft lip 9.9
749 acute mountain sickness 9.9
750 antisynthetase syndrome 9.9
751 pediatric hypertension 9.9
752 primary biliary cholangitis 9.9
753 soft tissue sarcoma 9.9
754 obsolete: atypical teratoid/rhabdoid tumor 9.9
755 hematopoietic stem cell transplantation 9.9
756 tetralogy of fallot 9.9
757 urate oxidase, pseudogene 9.9
758 myasthenia gravis 9.9
759 3-methylglutaconic aciduria, type iii 9.9
760 thymoma, familial 9.9
761 suppression of tumorigenicity 12 9.9
762 huntington disease-like 1 9.9
763 mycobacterium tuberculosis 1 9.9
764 hypertension, diastolic 9.9
765 preterm premature rupture of the membranes 9.9
766 cholangiocarcinoma 9.9
767 congenital hypothyroidism 9.9
768 familial adenomatous polyposis 9.9
769 brachydactyly 9.9
770 secondary progressive multiple sclerosis 9.9
771 ptosis 9.9
772 adenoid hypertrophy 9.9
773 cerebral artery occlusion 9.9
774 short bowel syndrome 9.9
775 asphyxia neonatorum 9.9
776 portal vein thrombosis 9.9
777 choledocholithiasis 9.9
778 varicocele 9.9
779 tuberous sclerosis 9.9
780 generalized anxiety disorder 9.9
781 gonadal dysgenesis 9.9
782 transient cerebral ischemia 9.9
783 astrocytoma 9.9
784 thymoma 9.9
785 breast disease 9.9
786 turner syndrome 9.9
787 radiculopathy 9.9
788 intrahepatic cholangiocarcinoma 9.9
789 myocarditis 9.9
790 fundus dystrophy 9.9
791 central sleep apnea 9.9
792 exophthalmos 9.9
793 necrotizing fasciitis 9.9
794 acute graft versus host disease 9.9
795 obsolete: combined hyperlipidemia 9.9
796 inherited retinal disorder 9.9
797 acute liver failure 9.9
798 aniridia 1 9.8
799 hepatic adenomas, familial 9.8
800 leukemia, chronic lymphocytic 9.8
801 tuberous sclerosis 1 9.8
802 wilms tumor 1 9.8
803 ascites, chylous 9.8
804 immune deficiency disease 9.8
805 aspirin resistance 9.8
806 leukemia, chronic myeloid 9.8
807 microphthalmia, syndromic 10 9.8
808 body mass index quantitative trait locus 13 9.8
809 aspergillosis 9.8
810 glucocorticoid resistance, generalized 9.8
811 hyperproinsulinemia 9.8
812 familial partial lipodystrophy 9.8
813 hyperphosphatemia 9.8
814 female breast cancer 9.8
815 idiopathic scoliosis 9.8
816 myelomeningocele 9.8
817 pollen allergy 9.8
818 sarcoma 9.8
819 cholecystolithiasis 9.8
820 primary biliary cirrhosis 9.8
821 prostatitis 9.8
822 urticaria 9.8
823 spondylosis 9.8
824 cystadenoma 9.8
825 interstitial lung disease 9.8
826 gastric dilatation 9.8
827 teratoma 9.8
828 fibrosarcoma 9.8
829 liposarcoma 9.8
830 myopathy 9.8
831 spindle cell sarcoma 9.8
832 myofibroma 9.8
833 movement disease 9.8
834 borna disease 9.8
835 aortic valve insufficiency 9.8
836 meningitis 9.8
837 encephalitis 9.8
838 placental abruption 9.8
839 pulmonary emphysema 9.8
840 hemophilia 9.8
841 myotonic dystrophy 9.8
842 brain tumor, childhood 9.8
843 familial glucocorticoid deficiency 9.8
844 leukemia, b-cell, chronic 9.8
845 mast cell activation syndrome 9.8
846 myotonia atrophica 9.8
847 pediatric multiple sclerosis 9.8
848 cerebral beriberi 9.8
849 angelman syndrome 9.8
850 lipomatosis, multiple symmetric 9.8
851 lipomatosis, multiple 9.8
852 small cell cancer of the lung 9.8
853 chromosome 2q35 duplication syndrome 9.8
854 wolfram syndrome 1 9.8
855 enterocolitis 9.8
856 myxedema 9.8
857 neuroblastoma 1 9.8
858 pituitary hormone deficiency, combined, 2 9.8
859 phobia, specific 9.8
860 human immunodeficiency virus type 1 9.8
861 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 9.8
862 chronic ulcer of skin 9.8
863 androgenic alopecia 9.8
864 oppositional defiant disorder 9.8
865 follicular lymphoma 9.8
866 colon adenoma 9.8
867 crohn's colitis 9.8
868 ectopic pregnancy 9.8
869 pelvic inflammatory disease 9.8
870 osteomyelitis 9.8
871 pleomorphic lipoma 9.8
872 meningoencephalitis 9.8
873 thrombotic thrombocytopenic purpura 9.8
874 hypospadias 9.8
875 depersonalization disorder 9.8
876 cauda equina syndrome 9.8
877 oligohydramnios 9.8
878 hypochondriasis 9.8
879 hyperinsulinemic hypoglycemia 9.8
880 premature ejaculation 9.8
881 cystitis 9.8
882 optic nerve disease 9.8
883 rectum adenocarcinoma 9.8
884 colon adenocarcinoma 9.8
885 sensory peripheral neuropathy 9.8
886 glycogen storage disease 9.8
887 pulmonary tuberculosis 9.8
888 mediastinal lipomatosis 9.8
889 tricuspid valve insufficiency 9.8
890 hypertrichosis 9.8
891 lymphocele 9.8
892 folliculitis 9.8
893 calciphylaxis 9.8
894 neurotic disorder 9.8
895 adjustment disorder 9.8
896 intestinal disease 9.8
897 colonic disease 9.8
898 acute pyelonephritis 9.8
899 adrenal adenoma 9.8
900 juvenile rheumatoid arthritis 9.8
901 monoclonal gammopathy of uncertain significance 9.8
902 active peptic ulcer disease 9.8
903 childhood leukemia 9.8
904 osteochondrosis 9.8
905 polyhydramnios 9.8
906 chronic fatigue syndrome 9.8
907 plantar fasciitis 9.8
908 kidney hypertrophy 9.8
909 disorders of gnas inactivation 9.8
910 amyloidosis aa 9.8
911 encephalocele 9.8
912 glioma 9.8
913 pure autonomic failure 9.8
914 splenomegaly 9.8
915 opioid addiction 9.8
916 posttransplant acute limbic encephalitis 9.8
917 glial tumor 9.8
918 acute sensory ataxic neuropathy 9.8
919 progressive familial heart block, type ia 9.7
920 maturity-onset diabetes of the young, type 1 9.7
921 macroglossia 9.7
922 neutrophil migration 9.7
923 optic atrophy 1 9.7
924 pilonidal sinus 9.7
925 scoliosis, isolated 1 9.7
926 thyroid cancer, nonmedullary, 1 9.7
927 acrocallosal syndrome 9.7
928 central hypoventilation syndrome, congenital 9.7
929 osteogenic sarcoma 9.7
930 phenylketonuria 9.7
931 lysosomal acid lipase deficiency 9.7
932 paine syndrome 9.7
933 androgen insensitivity, partial 9.7
934 chudley-mccullough syndrome 9.7
935 platelet glycoprotein iv deficiency 9.7
936 acute promyelocytic leukemia 9.7
937 myelodysplastic syndrome 9.7
938 peripartum cardiomyopathy 9.7
939 small cell carcinoma 9.7
940 colorectal adenocarcinoma 9.7
941 withdrawal disorder 9.7
942 omphalocele 9.7
943 migraine with aura 9.7
944 meconium aspiration syndrome 9.7
945 t cell deficiency 9.7
946 disseminated intravascular coagulation 9.7
947 adult respiratory distress syndrome 9.7
948 mitral valve insufficiency 9.7
949 diabetic autonomic neuropathy 9.7
950 pica disease 9.7
951 bile reflux 9.7
952 guillain-barre syndrome 9.7
953 kwashiorkor 9.7
954 somatization disorder 9.7
955 alcoholic liver cirrhosis 9.7
956 renal tubular acidosis 9.7
957 sclerosing cholangitis 9.7
958 heart septal defect 9.7
959 gastroenteritis 9.7
960 post-thrombotic syndrome 9.7
961 hemangioma 9.7
962 acquired polycythemia 9.7
963 tracheal stenosis 9.7
964 histiocytosis 9.7
965 pleural empyema 9.7
966 placental insufficiency 9.7
967 thyroid gland papillary carcinoma 9.7
968 dystonia 9.7
969 acquired immunodeficiency syndrome 9.7
970 premenstrual tension 9.7
971 measles 9.7
972 duodenitis 9.7
973 subacute delirium 9.7
974 perinatal necrotizing enterocolitis 9.7
975 decubitus ulcer 9.7
976 in situ carcinoma 9.7
977 bacterial pneumonia 9.7
978 atrophic gastritis 9.7
979 gas gangrene 9.7
980 homocystinuria 9.7
981 status asthmaticus 9.7
982 biliary tract disease 9.7
983 isolated gonadotropin-releasing hormone deficiency 9.7
984 aortic coarctation 9.7
985 familial hypertension 9.7
986 fournier gangrene 9.7
987 hair-an syndrome 9.7
988 meralgia paresthetica 9.7
989 prosthetic joint infection 9.7
990 tuberculous meningitis 9.7
991 abdominal wall defect 9.7
992 clopidogrel resistance 9.7
993 cytomegalovirus infection 9.7
994 cerebral malformation 9.7
995 cleft lip/palate 9.7
996 cerebrofacial arteriovenous metameric syndrome 9.7
997 pouchitis 9.7
998 non-acquired combined pituitary hormone deficiency 9.7
999 thyroid tumor 9.7
1000 pfeiffer syndrome 9.7
1001 coffin-siris syndrome 1 9.7
1002 hypertelorism 9.7
1003 kaposi sarcoma 9.7
1004 polykaryocytosis inducer 9.7
1005 dowling-degos disease 1 9.7
1006 strabismus 9.7
1007 digeorge syndrome 9.7
1008 suppressor of tumorigenicity 3 9.7
1009 renal hypodysplasia/aplasia 1 9.7
1010 vesicoureteral reflux 1 9.7
1011 adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency 9.7
1012 galactorrhea 9.7
1013 niemann-pick disease, type c1 9.7
1014 pseudovaginal perineoscrotal hypospadias 9.7
1015 fragile x syndrome 9.7
1016 muscular dystrophy, duchenne type 9.7
1017 premature ovarian failure 1 9.7
1018 kearns-sayre syndrome 9.7
1019 frontotemporal dementia 9.7
1020 pituitary adenoma, prolactin-secreting 9.7
1021 intervertebral disc disease 9.7
1022 mammographic density 9.7
1023 myopathy, myosin storage, autosomal dominant 9.7
1024 coronary heart disease 7 9.7
1025 alpha-1-antitrypsin deficiency 9.7
1026 cholangitis, primary sclerosing 9.7
1027 fanconi anemia, complementation group l 9.7
1028 accelerated tumor formation 9.7
1029 pachyonychia congenita 3 9.7
1030 hypophosphatemia 9.7
1031 orofacial cleft 9.7
1032 paraganglioma 9.7
1033 cone dystrophy 9.7
1034 body dysmorphic disorder 9.7
1035 drug allergy 9.7
1036 isolated growth hormone deficiency 9.7
1037 polycystic kidney disease 9.7
1038 keratoconus 9.7
1039 xerophthalmia 9.7
1040 tonsillitis 9.7
1041 nasopharyngitis 9.7
1042 cardia cancer 9.7
1043 microphthalmia 9.7
1044 salivary gland disease 9.7
1045 multiple personality disorder 9.7
1046 antisocial personality disorder 9.7
1047 hemiplegia 9.7
1048 esophageal varix 9.7
1049 hemopericardium 9.7
1050 penile cancer 9.7
1051 cornelia de lange syndrome 9.7
1052 pericardial effusion 9.7
1053 myopia 9.7
1054 coronary thrombosis 9.7
1055 chagas disease 9.7
1056 neurogenic bladder 9.7
1057 paranoid schizophrenia 9.7
1058 dysentery 9.7
1059 pathological gambling 9.7
1060 pancytopenia 9.7
1061 diabetic polyneuropathy 9.7
1062 keratoconjunctivitis sicca 9.7
1063 carotid stenosis 9.7
1064 uveitis 9.7
1065 diabetic cataract 9.7
1066 megaloblastic anemia 9.7
1067 squamous cell papilloma 9.7
1068 bacteriuria 9.7
1069 niemann-pick disease 9.7
1070 endogenous depression 9.7
1071 ventricular septal defect 9.7
1072 neuroendocrine tumor 9.7
1073 ocular melanoma 9.7
1074 mitral valve stenosis 9.7
1075 pericarditis 9.7
1076 neonatal jaundice 9.7
1077 gangliocytoma 9.7
1078 cystic teratoma 9.7
1079 myoma 9.7
1080 long qt syndrome 9.7
1081 bronchiolitis 9.7
1082 cystic kidney disease 9.7
1083 anuria 9.7
1084 antiphospholipid syndrome 9.7
1085 glioblastoma multiforme 9.7
1086 aspiration pneumonitis 9.7
1087 carotid artery disease 9.7
1088 duodenal obstruction 9.7
1089 lynch syndrome 9.7
1090 ganglioneuroma 9.7
1091 esophagus adenocarcinoma 9.7
1092 poliomyelitis 9.7
1093 arteriolosclerosis 9.7
1094 urinary tract obstruction 9.7
1095 ovarian serous cystadenocarcinoma 9.7
1096 conjunctivitis 9.7
1097 thyroid hyalinizing trabecular adenoma 9.7
1098 inflammatory breast carcinoma 9.7
1099 peroneal nerve paralysis 9.7
1100 paralytic ileus 9.7
1101 choline deficiency disease 9.7
1102 dermatophytosis 9.7
1103 cervix uteri carcinoma in situ 9.7
1104 mechanical strabismus 9.7
1105 dacryoadenitis 9.7
1106 polyarteritis nodosa 9.7
1107 mitochondrial disorders 9.7
1108 sickle cell disease 9.7
1109 autoimmune encephalitis 9.7
1110 biliary tract cancer 9.7
1111 carcinoma showing thymus-like differentiation 9.7
1112 cerebrospinal fluid leak 9.7
1113 cervical intraepithelial neoplasia 9.7
1114 chromosome 15q deletion 9.7
1115 cluster headache 9.7
1116 fasting hypoglycemia 9.7
1117 glioblastoma 9.7
1118 lichen sclerosus 9.7
1119 pilocytic astrocytoma 9.7
1120 single ventricular heart 9.7
1121 sudden sensorineural hearing loss 9.7
1122 transposition of the great arteries 9.7
1123 bunion 9.7
1124 anoxia 9.7
1125 cerebral atrophy 9.7
1126 dysautonomia 9.7
1127 foot drop 9.7
1128 hypertonia 9.7
1129 infantile hypotonia 9.7
1130 perioral myoclonia with absences 9.7
1131 inflammatory myopathy with abundant macrophages 9.7
1132 periodic paralysis 9.7
1133 virus-associated trichodysplasia spinulosa 9.7
1134 malignant tumor of penis 9.7
1135 obsolete: squamous cell carcinoma of head and neck 9.7
1136 benign idiopathic neonatal seizures 9.7
1137 maternal uniparental disomy 9.7
1138 cerebral amyloid angiopathy, cst3-related 9.6
1139 amyotrophic lateral sclerosis 1 9.6
1140 blood group--newfoundland 9.6
1141 cardiomyopathy, familial hypertrophic, 2 9.6
1142 coloboma of macula 9.6
1143 cornelia de lange syndrome 1 9.6
1144 diabetes mellitus, insulin-dependent, 2 9.6
1145 earlobe crease 9.6
1146 beckwith-wiedemann syndrome 9.6
1147 lateral meningocele syndrome 9.6
1148 erythermalgia, primary 9.6
1149 factor viii deficiency 9.6
1150 glaucoma, primary open angle 9.6
1151 hand skill, relative 9.6
1152 diaphragmatic hernia, congenital 9.6
1153 laryngomalacia 9.6
1154 legg-calve-perthes disease 9.6
1155 myositis 9.6
1156 neurofibromatosis, type iv, of riccardi 9.6
1157 neutrophilia, hereditary 9.6
1158 optic nerve hypoplasia, bilateral 9.6
1159 papillomatosis, confluent and reticulated 9.6
1160 parkinson disease, late-onset 9.6
1161 retinal detachment 9.6
1162 syringomyelia, noncommunicating isolated 9.6
1163 temporal arteritis 9.6
1164 thrombophilia due to activated protein c resistance 9.6
1165 trigeminal neuralgia 9.6
1166 williams-beuren syndrome 9.6
1167 joubert syndrome 1 9.6
1168 schopf-schulz-passarge syndrome 9.6
1169 enterokinase deficiency 9.6
1170 gastroschisis 9.6
1171 hyperlipoproteinemia, type i 9.6
1172 leprosy 3 9.6
1173 chylomicron retention disease 9.6
1174 methane production 9.6
1175 multiple pterygium syndrome, lethal type 9.6
1176 polycythemia vera 9.6
1177 enhanced s-cone syndrome 9.6
1178 sjogren syndrome 9.6
1179 asplenia, isolated congenital 9.6
1180 sudden infant death syndrome 9.6
1181 hypothyroidism, congenital, nongoitrous, 4 9.6
1182 wernicke-korsakoff syndrome 9.6
1183 hemophilia a 9.6
1184 mental retardation-hypotonic facies syndrome, x-linked, 1 9.6
1185 rett syndrome 9.6
1186 retinitis pigmentosa 11 9.6
1187 maturity-onset diabetes of the young, type 3 9.6
1188 abcd syndrome 9.6
1189 leptin, serum level of, quantitative trait locus 1 9.6
1190 astigmatism 9.6
1191 brittle bone disorder 9.6
1192 sickle cell anemia 9.6
1193 progressive familial heart block, type ib 9.6
1194 langerhans cell histiocytosis 9.6
1195 anisomastia 9.6
1196 alveolar soft part sarcoma 9.6
1197 chromosome 1p36 deletion syndrome 9.6
1198 hypertensive nephropathy 9.6
1199 asthma-related traits 2 9.6
1200 testicular microlithiasis 9.6
1201 asthma-related traits 4 9.6
1202 malaria 9.6
1203 intraocular pressure quantitative trait locus 9.6
1204 cavitary optic disc anomalies 9.6
1205 chromosome 16p11.2 deletion syndrome, 593-kb 9.6
1206 plasminogen activator inhibitor-1 deficiency 9.6
1207 myxoid liposarcoma 9.6
1208 macrostomia, isolated 9.6
1209 complement component 3 deficiency, autosomal recessive 9.6
1210 retinal arterial macroaneurysm with supravalvular pulmonic stenosis 9.6
1211 glycerol quantitative trait locus 9.6
1212 ras-associated autoimmune leukoproliferative disorder 9.6
1213 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 9.6
1214 bainbridge-ropers syndrome 9.6
1215 alkuraya-kucinskas syndrome 9.6
1216 neuropathy, congenital hypomyelinating, 2 9.6
1217 hypertrophic scars 9.6
1218 tendinosis 9.6
1219 bacterial sepsis 9.6
1220 autoimmune peripheral neuropathy 9.6
1221 invasive aspergillosis 9.6
1222 asperger syndrome 9.6
1223 distal arthrogryposis 9.6
1224 zollinger-ellison syndrome 9.6
1225 atrioventricular block 9.6
1226 hemorrhagic cystitis 9.6
1227 fibroma 9.6
1228 infective endocarditis 9.6
1229 interleukin-7 receptor alpha deficiency 9.6
1230 pervasive developmental disorder 9.6
1231 microscopic colitis 9.6
1232 ileitis 9.6
1233 ileocolitis 9.6
1234 stuttering 9.6
1235 tracheomalacia 9.6
1236 anal fistula 9.6
1237 transient neonatal diabetes mellitus 9.6
1238 myoglobinuria 9.6
1239 lymphoblastic lymphoma 9.6
1240 type 1 diabetes mellitus 2 9.6
1241 endometrial disease 9.6
1242 osteonecrosis 9.6
1243 left bundle branch hemiblock 9.6
1244 endocarditis 9.6
1245 lactose intolerance 9.6
1246 interstitial nephritis 9.6
1247 wolfram syndrome 9.6
1248 open-angle glaucoma 9.6
1249 chronic pyelonephritis 9.6
1250 obsessive-compulsive personality disorder 9.6
1251 placenta praevia 9.6
1252 allergic conjunctivitis 9.6
1253 spondyloarthropathy 9.6
1254 microcytic anemia 9.6
1255 rabies 9.6
1256 erysipelas 9.6
1257 tetanus 9.6
1258 megacolon 9.6
1259 constrictive pericarditis 9.6
1260 neonatal diabetes mellitus 9.6
1261 lyme disease 9.6
1262 mononeuropathy 9.6
1263 lymphocytic choriomeningitis 9.6
1264 graves' disease 9.6
1265 bronchopneumonia 9.6
1266 hepatitis a 9.6
1267 acute kidney tubular necrosis 9.6
1268 nephrocalcinosis 9.6
1269 telangiectasis 9.6
1270 migraine without aura 9.6
1271 endomyocardial fibrosis 9.6
1272 renal osteodystrophy 9.6
1273 hellp syndrome 9.6
1274 megaesophagus 9.6
1275 right bundle branch block 9.6
1276 exocrine pancreatic insufficiency 9.6
1277 osteopetrosis 9.6
1278 obstructive jaundice 9.6
1279 biliary atresia 9.6
1280 patent foramen ovale 9.6
1281 sick sinus syndrome 9.6
1282 familial lipoprotein lipase deficiency 9.6
1283 oligospermia 9.6
1284 pyuria 9.6
1285 hypersensitivity reaction type iii disease 9.6
1286 rheumatic fever 9.6
1287 renovascular hypertension 9.6
1288 calcinosis 9.6
1289 urethral stricture 9.6
1290 dysostosis 9.6
1291 thrombocytosis 9.6
1292 ankylosis 9.6
1293 lateral sclerosis 9.6
1294 craniosynostosis 9.6
1295 basal cell carcinoma 9.6
1296 hematologic cancer 9.6
1297 dermoid cyst 9.6
1298 transitional cell carcinoma 9.6
1299 lymphangiosarcoma 9.6
1300 phimosis 9.6
1301 tic disorder 9.6
1302 idiopathic interstitial pneumonia 9.6
1303 cranial nerve malignant neoplasm 9.6
1304 cervix carcinoma 9.6
1305 papillary carcinoma 9.6
1306 demyelinating disease 9.6
1307 syringomyelia 9.6
1308 temporal lobe epilepsy 9.6
1309 bone inflammation disease 9.6
1310 bacterial vaginosis 9.6
1311 mammary paget's disease 9.6
1312 breast adenocarcinoma 9.6
1313 necrobiosis lipoidica 9.6
1314 mastocytosis 9.6
1315 mast cell neoplasm 9.6
1316 pulmonary fibrosis 9.6
1317 male reproductive organ cancer 9.6
1318 restrictive cardiomyopathy 9.6
1319 duodenogastric reflux 9.6
1320 ganglioneuroblastoma 9.6
1321 pyoderma 9.6
1322 dyslexia 9.6
1323 holoprosencephaly 9.6
1324 extracutaneous mastocytoma 9.6
1325 brain edema 9.6
1326 essential tremor 9.6
1327 arteriosclerosis obliterans 9.6
1328 demyelinating polyneuropathy 9.6
1329 mature teratoma 9.6
1330 large intestine cancer 9.6
1331 connective tissue disease 9.6
1332 diffuse idiopathic skeletal hyperostosis 9.6
1333 delusional disorder 9.6
1334 gallbladder melanoma 9.6
1335 complement component 3 deficiency 9.6
1336 ariboflavinosis 9.6
1337 pellagra 9.6
1338 chickenpox 9.6
1339 skin melanoma 9.6
1340 autosomal dominant polycystic kidney disease 9.6
1341 hard palate cancer 9.6
1342 tracheitis 9.6
1343 lipid storage disease 9.6
1344 uterine corpus cancer 9.6
1345 bronchiectasis 9.6
1346 hydrocele 9.6
1347 toxoplasmosis 9.6
1348 16p11.2 recurrent microdeletion 9.6
1349 bap1 tumor predisposition syndrome 9.6
1350 col1a1/2-related osteogenesis imperfecta 9.6
1351 multiple epiphyseal dysplasia, recessive 9.6
1352 complete androgen insensitivity syndrome 9.6
1353 germ cells tumors 9.6
1354 gigantism 9.6
1355 glucagonoma 9.6
1356 hansen's disease 9.6
1357 hypoadrenalism 9.6
1358 lymphomatous thyroiditis 9.6
1359 neural crest tumor 9.6
1360 pituitary stalk interruption syndrome 9.6
1361 pseudobulbar affect 9.6
1362 scleredema 9.6
1363 raynaud phenomenon 9.6
1364 aldosterone-producing adenoma 9.6
1365 multiple endocrine neoplasia 9.6
1366 cerebral hypoxia 9.6
1367 febrile seizures 9.6
1368 uniparental disomy of chromosome 15 9.6
1369 uniparental disomy of chromosome 1 9.6
1370 severe early-childhood-onset retinal dystrophy 9.6
1371 arterial thoracic outlet syndrome 9.6
1372 paracetamol poisoning 9.6
1373 chronic enteropathy associated with slco2a1 gene 9.6
1374 avascular necrosis 9.6
1375 congenital amyoplasia 9.6
1376 recurrent acute pancreatitis 9.6
1377 primary lymphedema 9.6
1378 serotonin syndrome 9.6
1379 rare tumor 9.6
1380 acth-independent cushing syndrome 9.6
1381 abducens palsy 9.4
1382 anisocoria 9.4
1383 arteriovenous malformations of the brain 9.4
1384 machado-joseph disease 9.4
1385 sotos syndrome 1 9.4
1386 coarctation of aorta 9.4
1387 creutzfeldt-jakob disease 9.4
1388 dens evaginatus 9.4
1389 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.4
1390 major affective disorder 1 9.4
1391 multiple endocrine neoplasia, type i 9.4
1392 camurati-engelmann disease 9.4
1393 pilomatrixoma 9.4
1394 exostoses, multiple, type ii 9.4
1395 lymphoma, mucosa-associated lymphoid type 9.4
1396 gilles de la tourette syndrome 9.4
1397 hemifacial spasm, familial 9.4
1398 congenital anomalies of kidney and urinary tract 2 9.4
1399 hyperalphalipoproteinemia 1 9.4
1400 gilbert syndrome 9.4
1401 hyperlipoproteinemia, type iv 9.4
1402 hyperparathyroidism 1 9.4
1403 hypogonadotropic hypogonadism 7 with or without anosmia 9.4
1404 multiple system atrophy 1 9.4
1405 keloid formation 9.4
1406 leiomyoma, uterine 9.4
1407 lentigines 9.4
1408 li-fraumeni syndrome 9.4
1409 marfan syndrome 9.4
1410 thyroid carcinoma, familial medullary 9.4
1411 medulloblastoma 9.4
1412 melanoma, uveal 9.4
1413 moebius syndrome 9.4
1414 nondisjunction 9.4
1415 motion sickness 9.4
1416 cowden syndrome 1 9.4
1417 noonan syndrome 1 9.4
1418 osseous heteroplasia, progressive 9.4
1419 pancreas, dorsal, agenesis of 9.4
1420 andersen cardiodysrhythmic periodic paralysis 9.4
1421 hypokalemic periodic paralysis, type 1 9.4
1422 platelet membrane fluidity 9.4
1423 polydactyly, postaxial, type a1 9.4
1424 hutchinson-gilford progeria syndrome 9.4
1425 pulmonary fibrosis, idiopathic 9.4
1426 pulmonary hemosiderosis 9.4
1427 raynaud disease 9.4
1428 spinocerebellar ataxia 2 9.4
1429 odontochondrodysplasia 9.4
1430 spondylosis, cervical 9.4
1431 stiff-person syndrome 9.4
1432 thrombocytopenic purpura, autoimmune 9.4
1433 thyroid hormone resistance, generalized, autosomal dominant 9.4
1434 tracheoesophageal fistula with or without esophageal atresia 9.4
1435 trichorhinophalangeal syndrome, type i 9.4
1436 uterine anomalies 9.4
1437 cardiomyopathy, familial hypertrophic, 1 9.4
1438 vitiligo-associated multiple autoimmune disease susceptibility 6 9.4
1439 wolf-hirschhorn syndrome 9.4
1440 adrenocortical carcinoma, hereditary 9.4
1441 tangier disease 9.4
1442 arterial tortuosity syndrome 9.4
1443 ataxia-telangiectasia 9.4
1444 c syndrome 9.4
1445 cardiomyopathy, dilated, with hypergonadotropic hypogonadism 9.4
1446 congenital heart defects, hamartomas of tongue, and polysyndactyly 9.4
1447 corpus callosum, agenesis of 9.4
1448 costello syndrome 9.4
1449 craniosynostosis with fibular aplasia 9.4
1450 mitochondrial complex iv deficiency 9.4
1451 leukoencephalopathy, hereditary diffuse, with spheroids 9.4
1452 diastrophic dysplasia 9.4
1453 duodenal atresia 9.4
1454 ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive 9.4
1455 fanconi anemia, complementation group c 9.4
1456 fanconi anemia, complementation group a 9.4
1457 fructose utilization 9.4
1458 gaucher disease, type i 9.4
1459 multiple acyl-coa dehydrogenase deficiency 9.4
1460 halothane hepatitis 9.4
1461 hydrocephalus, congenital, 1 9.4
1462 hydrocephalus due to congenital stenosis of aqueduct of sylvius 9.4
1463 hypoadrenocorticism, familial 9.4
1464 autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia 9.4
1465 cholestasis, benign recurrent intrahepatic, 1 9.4
1466 laurence-moon syndrome 9.4
1467 familial mediterranean fever 9.4
1468 spinal muscular atrophy, type iii 9.4
1469 myeloperoxidase deficiency 9.4
1470 myopathy, myosin storage, autosomal recessive 9.4
1471 neuraminidase deficiency 9.4
1472 hyperoxaluria, primary, type i 9.4
1473 hyperoxaluria, primary, type ii 9.4
1474 short-rib thoracic dysplasia 6 with or without polydactyly 9.4
1475 pulmonic stenosis 9.4
1476 pycnodysostosis 9.4
1477 inflammatory bowel disease 1 9.4
1478 respiratory distress syndrome in premature infants 9.4
1479 hemophagocytic lymphohistiocytosis, familial, 1 9.4
1480 short syndrome 9.4
1481 sodium-potassium-atpase activity of red cell 9.4
1482 succinic semialdehyde dehydrogenase deficiency 9.4
1483 taurodontism 9.4
1484 thyrotropin-releasing hormone deficiency 9.4
1485 hypothyroidism, congenital, nongoitrous, 1 9.4
1486 werner syndrome 9.4
1487 wilson disease 9.4
1488 muscular dystrophy, becker type 9.4
1489 atkin-flaitz syndrome 9.4
1490 cornelia de lange syndrome 5 9.4
1491 tubulin, beta 9.4
1492 choroideremia 9.4
1493 choroideremia, deafness, and mental retardation 9.4
1494 coffin-lowry syndrome 9.4
1495 deafness, x-linked 2 9.4
1496 glycerol kinase deficiency 9.4
1497 hypoparathyroidism, x-linked 9.4
1498 mental retardation with optic atrophy, deafness, and seizures 9.4
1499 diabetes and deafness, maternally inherited 9.4
1500 gonadal agenesis 9.4
1501 fryns microphthalmia syndrome 9.4
1502 hypocalcemia, autosomal dominant 1 9.4
1503 autoimmune lymphoproliferative syndrome 9.4
1504 ossification of the posterior longitudinal ligament of spine 9.4
1505 psoriasis 2 9.4
1506 bile duct cysts 9.4
1507 pseudohypoparathyroidism, type ib 9.4
1508 papillary thyroid microcarcinoma 9.4
1509 microvascular complications of diabetes 1 9.4
1510 hypoalphalipoproteinemia, primary, 1 9.4
1511 mitochondrial complex v deficiency, nuclear type 1 9.4
1512 aceruloplasminemia 9.4
1513 rheumatoid arthritis, systemic juvenile 9.4
1514 orthostatic intolerance 9.4
1515 paragangliomas 3 9.4
1516 late-onset retinal degeneration 9.4
1517 fasting insulin level quantitative trait locus 1 9.4
1518 diamond-blackfan anemia 2 9.4
1519 atrioventricular septal defect 9.4
1520 maturity-onset diabetes of the young, type 4 9.4
1521 vitiligo-associated multiple autoimmune disease susceptibility 1 9.4
1522 lipodystrophy, familial partial, type 7 9.4
1523 spermatogenic failure 3 9.4
1524 adiponectin, serum level of, quantitative trait locus 2 9.4
1525 adiponectin, serum level of, quantitative trait locus 3 9.4
1526 nasopharyngeal carcinoma 9.4
1527 asthma-related traits 1 9.4
1528 epidermolysis bullosa simplex superficialis 9.4
1529 niemann-pick disease, type c2 9.4
1530 peeling skin syndrome 4 9.4
1531 neutrophilic dermatosis, acute febrile 9.4
1532 tropical calcific pancreatitis 9.4
1533 kala-azar 1 9.4
1534 slowed nerve conduction velocity, autosomal dominant 9.4
1535 parathyroid carcinoma 9.4
1536 coronary heart disease 4 9.4
1537 myocardial infarction 2 9.4
1538 lipodystrophy, congenital generalized, type 1 9.4
1539 transposition of the great arteries, dextro-looped 1 9.4
1540 carney complex variant 9.4
1541 telomere length, mean leukocyte 9.4
1542 aplastic anemia 9.4
1543 li-fraumeni syndrome 2 9.4
1544 syndactyly, mesoaxial synostotic, with phalangeal reduction 9.4
1545 esophagitis, eosinophilic, 1 9.4
1546 potocki-lupski syndrome 9.4
1547 skin/hair/eye pigmentation, variation in, 9 9.4
1548 kawasaki disease 9.4
1549 alopecia, neurologic defects, and endocrinopathy syndrome 9.4
1550 trehalase deficiency 9.4
1551 myd88 deficiency 9.4
1552 joubert syndrome 8 9.4
1553 lipodystrophy, congenital generalized, type 3 9.4
1554 lung cancer susceptibility 3 9.4
1555 microvascular complications of diabetes 2 9.4
1556 polymicrogyria, bilateral temporooccipital 9.4
1557 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.4
1558 premature ovarian failure 7 9.4
1559 short sleeper 9.4
1560 hearing loss, noise-induced 9.4
1561 antithrombin iii deficiency 9.4
1562 trichotillomania 9.4
1563 tuberous sclerosis 2 9.4
1564 brachydactyly, type e2 9.4
1565 autism 17 9.4
1566 dengue virus 9.4
1567 cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 9.4
1568 membranous nephropathy 9.4
1569 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 9.4
1570 monocarboxylate transporter 1 deficiency 9.4
1571 chronic mountain sickness 9.4
1572 seizures, scoliosis, and macrocephaly/microcephaly syndrome 9.4
1573 chorea, childhood-onset, with psychomotor retardation 9.4
1574 aniridia 2 9.4
1575 renal hypodysplasia/aplasia 3 9.4
1576 central centrifugal cicatricial alopecia 9.4
1577 fetal akinesia deformation sequence 3 9.4
1578 adrenal cortical carcinoma 9.4
1579 autoimmune uveitis 9.4
1580 autoimmune gastritis 9.4
1581 chikungunya 9.4
1582 arrhythmogenic right ventricular cardiomyopathy 9.4
1583 periventricular nodular heterotopia 9.4
1584 multinodular goiter 9.4
1585 congenital generalized lipodystrophy 9.4
1586 severe congenital neutropenia 9.4
1587 tooth agenesis 9.4
1588 extrapulmonary tuberculosis 9.4
1589 hypochromic microcytic anemia 9.4
1590 fetal alcohol syndrome 9.4
1591 alcohol-related birth defect 9.4
1592 spastic cerebral palsy 9.4
1593 fetal alcohol spectrum disorder 9.4
1594 mantle cell lymphoma 9.4
1595 third-degree atrioventricular block 9.4
1596 sinoatrial node disease 9.4
1597 oral squamous cell carcinoma 9.4
1598 pancreatic agenesis 9.4
1599 adrenal cortical adenoma 9.4
1600 gastrointestinal carcinoma 9.4
1601 ovarian serous carcinoma 9.4
1602 munchausen by proxy 9.4
1603 ductal carcinoma in situ 9.4
1604 estrogen-receptor negative breast cancer 9.4
1605 gamma-amino butyric acid metabolism disorder 9.4
1606 ischemic colitis 9.4
1607 clostridium difficile colitis 9.4
1608 sclerosteosis 9.4
1609 autosomal dominant non-syndromic intellectual disability 9.4
1610 lung abscess 9.4
1611 respiratory allergy 9.4
1612 autoimmune neuropathy 9.4
1613 penicillin allergy 9.4
1614 spinal disease 9.4
1615 hyperekplexia 9.4
1616 autosomal dominant non-syndromic intellectual disability 1 9.4
1617 progressive familial intrahepatic cholestasis 9.4
1618 mucositis 9.4
1619 chronic myelomonocytic leukemia 9.4
1620 superior semicircular canal dehiscence 9.4
1621 cakut 9.4
1622 nodal marginal zone lymphoma 9.4
1623 mixed sleep apnea 9.4
1624 bronchiectasis 3 9.4
1625 nodular malignant melanoma 9.4
1626 cysticercosis 9.4
1627 pigmentation disease 9.4
1628 thymus lymphoma 9.4
1629 pleurisy 9.4
1630 mumps 9.4
1631 monocular esotropia 9.4
1632 siderosis 9.4
1633 blepharophimosis 9.4
1634 common cold 9.4
1635 esophageal atresia 9.4
1636 viral pneumonia 9.4
1637 supine hypotensive syndrome 9.4
1638 charcot-marie-tooth disease 9.4
1639 protein-losing enteropathy 9.4
1640 frontal sinusitis 9.4
1641 malignant hypertension 9.4
1642 voyeurism 9.4
1643 abducens nerve disease 9.4
1644 benign essential hypertension 9.4
1645 amnestic disorder 9.4
1646 lipoid nephrosis 9.4
1647 myiasis 9.4
1648 enophthalmos 9.4
1649 hypoparathyroidism 9.4
1650 opioid abuse 9.4
1651 appendix cancer 9.4
1652 arteriovenous malformation 9.4
1653 retinal microaneurysm 9.4
1654 schizophreniform disorder 9.4
1655 gingival recession 9.4
1656 functional diarrhea 9.4
1657 alternating exotropia 9.4
1658 exotropia 9.4
1659 sciatic neuropathy 9.4
1660 autonomic nervous system disease 9.4
1661 horner's syndrome 9.4
1662 suppurative otitis media 9.4
1663 rumination disorder 9.4
1664 hypertensive retinopathy 9.4
1665 emery-dreifuss muscular dystrophy 9.4
1666 chronic laryngitis 9.4
1667 hepatorenal syndrome 9.4
1668 tinea cruris 9.4
1669 synostosis 9.4
1670 pulmonary alveolar proteinosis 9.4
1671 common variable immunodeficiency 9.4
1672 descending colon cancer 9.4
1673 dengue hemorrhagic fever 9.4
1674 anisometropia 9.4
1675 cough variant asthma 9.4
1676 marasmus 9.4
1677 endocrine exophthalmos 9.4
1678 spinal muscular atrophy 9.4
1679 entropion 9.4
1680 intermittent explosive disorder 9.4
1681 tinea pedis 9.4
1682 hepatic coma 9.4
1683 hemolytic-uremic syndrome 9.4
1684 locked-in syndrome 9.4
1685 newborn respiratory distress syndrome 9.4
1686 cerebral atherosclerosis 9.4
1687 ancylostomiasis 9.4
1688 choreatic disease 9.4
1689 miller fisher syndrome 9.4
1690 central nervous system leukemia 9.4
1691 hereditary spherocytosis 9.4
1692 vertebrobasilar insufficiency 9.4
1693 balanitis 9.4
1694 mechanical entropion 9.4
1695 crescentic glomerulonephritis 9.4
1696 esophageal candidiasis 9.4
1697 allergic bronchopulmonary aspergillosis 9.4
1698 brain cancer 9.4
1699 nontoxic goiter 9.4
1700 nodular goiter 9.4
1701 intestinal tuberculosis 9.4
1702 congenital toxoplasmosis 9.4
1703 neurosarcoidosis 9.4
1704 hepatic encephalopathy 9.4
1705 coccidioidomycosis 9.4
1706 balanitis xerotica obliterans 9.4
1707 paranasal sinus disease 9.4
1708 hypermobility syndrome 9.4
1709 hypolipoproteinemia 9.4
1710 plasmodium falciparum malaria 9.4
1711 epicondylitis 9.4
1712 anus cancer 9.4
1713 frozen shoulder 9.4
1714 pulmonary valve insufficiency 9.4
1715 leopard syndrome 9.4
1716 pleuropneumonia 9.4
1717 critical illness polyneuropathy 9.4
1718 autosomal dominant cerebellar ataxia 9.4
1719 glossopharyngeal neuralgia 9.4
1720 root resorption 9.4
1721 foster-kennedy syndrome 9.4
1722 hereditary angioedema 9.4
1723 aggressive periodontitis 9.4
1724 cystic echinococcosis 9.4
1725 echinococcosis 9.4
1726 angioedema 9.4
1727 dermatomycosis 9.4
1728 thrombocytopenia due to platelet alloimmunization 9.4
1729 lymphadenitis 9.4
1730 benign breast phyllodes tumor 9.4
1731 ichthyosis 9.4
1732 retinal vein occlusion 9.4
1733 histoplasmosis 9.4
1734 factitious disorder 9.4
1735 islet cell tumor 9.4
1736 neuroendocrine carcinoma 9.4
1737 neuritis 9.4
1738 status epilepticus 9.4
1739 childhood absence epilepsy 9.4
1740 atrial heart septal defect 9.4
1741 gaucher's disease 9.4
1742 giant cell tumor 9.4
1743 hepatitis d 9.4
1744 heel spur 9.4
1745 ectodermal dysplasia 9.4
1746 tularemia 9.4
1747 vaginitis 9.4
1748 essential thrombocythemia 9.4
1749 focal epilepsy 9.4
1750 granulomatous hepatitis 9.4
1751 pharyngitis 9.4
1752 gonadal disease 9.4
1753 leptospirosis 9.4
1754 motor neuron disease 9.4
1755 generalized atherosclerosis 9.4
1756 macrocytic anemia 9.4
1757 relapsing-remitting multiple sclerosis 9.4
1758 glomus tumor 9.4
1759 hyperpituitarism 9.4
1760 central retinal vein occlusion 9.4
1761 protein s deficiency 9.4
1762 motor peripheral neuropathy 9.4
1763 enamel erosion 9.4
1764 testicular disease 9.4
1765 splenic abscess 9.4
1766 opiate dependence 9.4
1767 agammaglobulinemia 9.4
1768 adenomyoma 9.4
1769 leydig cell tumor 9.4
1770 hemangioma of liver 9.4
1771 skin atrophy 9.4
1772 auditory system disease 9.4
1773 acalculous cholecystitis 9.4
1774 bruxism 9.4
1775 laryngeal squamous cell carcinoma 9.4
1776 cryoglobulinemia 9.4
1777 membranoproliferative glomerulonephritis 9.4
1778 testicular cancer 9.4
1779 acinar cell carcinoma 9.4
1780 mucinous adenocarcinoma 9.4
1781 thoracic outlet syndrome 9.4
1782 gastrointestinal system cancer 9.4
1783 mucinoses 9.4
1784 neurilemmoma 9.4
1785 myelitis 9.4
1786 complex regional pain syndrome 9.4
1787 ovarian cystadenoma 9.4
1788 germinoma 9.4
1789 central nervous system disease 9.4
1790 osteitis fibrosa 9.4
1791 glycoproteinosis 9.4
1792 cranial nerve neoplasm 9.4
1793 cerebritis 9.4
1794 laryngitis 9.4
1795 superior mesenteric artery syndrome 9.4
1796 appendix adenocarcinoma 9.4
1797 cervical adenocarcinoma 9.4
1798 cervical squamous cell carcinoma 9.4
1799 protein c deficiency 9.4
1800 granuloma annulare 9.4
1801 posterior cerebral artery infarction 9.4
1802 colonic pseudo-obstruction 9.4
1803 vulvitis 9.4
1804 pituitary-dependent cushing's disease 9.4
1805 adrenal cortical adenocarcinoma 9.4
1806 thyroid gland medullary carcinoma 9.4
1807 bladder urothelial carcinoma 9.4
1808 linitis plastica 9.4
1809 erythrasma 9.4
1810 biliary dyskinesia 9.4
1811 syphilis 9.4
1812 rh isoimmunization 9.4
1813 systemic scleroderma 9.4
1814 mutism 9.4
1815 microsporidiosis 9.4
1816 polyradiculoneuropathy 9.4
1817 myofascial pain syndrome 9.4
1818 granulomatous dermatitis 9.4
1819 somatostatinoma 9.4
1820 pseudohypoaldosteronism 9.4
1821 bile duct cancer 9.4
1822 ulnar neuropathy 9.4
1823 placenta accreta 9.4
1824 vasculogenic impotence 9.4
1825 proliferative glomerulonephritis 9.4
1826 diffuse glomerulonephritis 9.4
1827 immune-complex glomerulonephritis 9.4
1828 trachea carcinoma 9.4
1829 gastroesophageal junction adenocarcinoma 9.4
1830 alcoholic pancreatitis 9.4
1831 optic nerve glioma 9.4
1832 ganglioglioma 9.4
1833 middle ear disease 9.4
1834 aortic disease 9.4
1835 anterograde amnesia 9.4
1836 pulmonary coin lesion 9.4
1837 functioning pituitary adenoma 9.4
1838 acute t cell leukemia 9.4
1839 retinal disease 9.4
1840 well-differentiated liposarcoma 9.4
1841 gastric liposarcoma 9.4
1842 median neuropathy 9.4
1843 pyosalpinx 9.4
1844 adult lymphoma 9.4
1845 hemolytic anemia 9.4
1846 silent myocardial infarction 9.4
1847 esophageal disease 9.4
1848 mitral valve disease 9.4
1849 cll/sll 9.4
1850 central pontine myelinolysis 9.4
1851 acral lentiginous melanoma 9.4
1852 double outlet right ventricle 9.4
1853 pulmonary valve stenosis 9.4
1854 bilateral breast cancer 9.4
1855 juvenile pilocytic astrocytoma 9.4
1856 hepatoblastoma 9.4
1857 skin tag 9.4
1858 mitochondrial metabolism disease 9.4
1859 anal canal squamous cell carcinoma 9.4
1860 axonal neuropathy 9.4
1861 peptic ulcer perforation 9.4
1862 parathyroid adenoma 9.4
1863 cocaine abuse 9.4
1864 chronic rhinitis 9.4
1865 scabies 9.4
1866 osteochondritis dissecans 9.4
1867 brachial plexus lesion 9.4
1868 cyclothymic disorder 9.4
1869 actinomycosis 9.4
1870 mucormycosis 9.4
1871 acute cor pulmonale 9.4
1872 monocytic leukemia 9.4
1873 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.4
1874 malignant hyperthermia 9.4
1875 pyoderma gangrenosum 9.4
1876 oropharynx cancer 9.4
1877 herpes simplex 9.4
1878 nervous system disease 9.4
1879 gastroduodenitis 9.4
1880 tongue cancer 9.4
1881 vein disease 9.4
1882 leukoplakia of penis 9.4
1883 actinic keratosis 9.4
1884 neuromyelitis optica 9.4
1885 rosacea 9.4
1886 severe nonproliferative diabetic retinopathy 9.4
1887 hepatopulmonary syndrome 9.4
1888 leishmaniasis 9.4
1889 visceral leishmaniasis 9.4
1890 speech disorder 9.4
1891 primary cerebellar degeneration 9.4
1892 ocular hypertension 9.4
1893 viral infectious disease 9.4
1894 keratoconjunctivitis 9.4
1895 iridocyclitis 9.4
1896 blepharitis 9.4
1897 dextrocardia 9.4
1898 krukenberg carcinoma 9.4
1899 senile cataract 9.4
1900 cervical incompetence 9.4
1901 tenosynovitis 9.4
1902 refractive error 9.4
1903 accommodative esotropia 9.4
1904 esotropia 9.4
1905 lymph node disease 9.4
1906 hypoplastic left heart syndrome 9.4
1907 cocaine dependence 9.4
1908 factor v leiden thrombophilia 9.4
1909 keloid disorder 9.4
1910 limb-girdle muscular dystrophy 9.4
1911 alk-related neuroblastic tumor susceptibility 9.4
1912 berardinelli-seip congenital lipodystrophy 9.4
1913 chd2-related neurodevelopmental disorders 9.4
1914 charcot-marie-tooth neuropathy type 2a 9.4
1915 cytochrome p450 oxidoreductase deficiency 9.4
1916 diabetes mellitus, 6q24-related transient neonatal 9.4
1917 fgfr-related craniosynostosis syndromes 9.4
1918 heritable pulmonary arterial hypertension 9.4
1919 hypermobile ehlers-danlos syndrome 9.4
1920 mbd5 haploinsufficiency 9.4
1921 prss1-related hereditary pancreatitis 9.4
1922 prothrombin-related thrombophilia 9.4
1923 rab18 deficiency 9.4
1924 47, xxy 9.4
1925 amaurosis fugax 9.4
1926 aminoaciduria 9.4
1927 anterior uveitis 9.4
1928 autoimmune atrophic gastritis 9.4
1929 autoimmune enteropathy 9.4
1930 autoimmune myocarditis 9.4
1931 binswanger's disease 9.4
1932 brittle diabetes 9.4
1933 broken heart syndrome 9.4
1934 cataract-glaucoma 9.4
1935 central congenital hypothyroidism 9.4
1936 chiari malformation 9.4
1937 chromosome 16q duplication 9.4
1938 chromosome 19q duplication 9.4
1939 chromosome 4p deletion 9.4
1940 chromosome 5p duplication 9.4
1941 chronic thromboembolic pulmonary hypertension 9.4
1942 congenitally corrected transposition of the great arteries 9.4
1943 coronary artery aneurysm 9.4
1944 depersonalization/derealization disorder 9.4
1945 diencephalic syndrome 9.4
1946 distal renal tubular acidosis 9.4
1947 dock2 deficiency 9.4
1948 double discordia 9.4
1949 elective mutism 9.4
1950 emery-dreifuss muscular dystrophy, x-linked 9.4
1951 familial colorectal cancer 9.4
1952 familial isolated hyperparathyroidism 9.4
1953 gas bloat syndrome 9.4
1954 hemophilic arthropathy 9.4
1955 hemorrhagic proctocolitis 9.4
1956 hemorrhagic shock and encephalopathy syndrome 9.4
1957 hereditary antithrombin deficiency 9.4
1958 homologous wasting disease 9.4
1959 horseshoe kidney 9.4
1960 idiopathic hypersomnia 9.4
1961 insulin-resistance type b 9.4
1962 itch e3 ubiquitin ligase deficiency 9.4
1963 jackhammer esophagus 9.4
1964 kikuchi disease 9.4
1965 klebsiella infection 9.4
1966 lymphangiectasis 9.4
1967 lymphosarcoma 9.4
1968 myoclonus epilepsy 9.4
1969 neonatal meningitis 9.4
1970 neuroendocrine carcinoma of the cervix 9.4
1971 nf-kappa b essential modulator deficiency 9.4
1972 oral cancer 9.4
1973 pachygyria 9.4
1974 pancreatitis, pediatric 9.4
1975 papular mucinosis 9.4
1976 plasmablastic lymphoma 9.4
1977 post-traumatic epilepsy 9.4
1978 progressive transformation of germinal centers 9.4
1979 pseudo-turner syndrome 9.4
1980 retinitis pigmentosa 2, x-linked 9.4
1981 retinochoroidal coloboma 9.4
1982 ring chromosome 13 9.4
1983 secondary adrenal insufficiency 9.4
1984 severe x-linked intellectual disability, gustavson type 9.4
1985 skeletal dysplasias 9.4
1986 sudden arrhythmia death syndrome 9.4
1987 supraglottic laryngeal cancer 9.4
1988 talipes equinovarus 9.4
1989 thyrotoxic periodic paralysis 9.4
1990 transverse myelitis 9.4
1991 trochlear dysplasia 9.4
1992 uniparental disomy of chromosome 2 9.4
1993 uterine sarcoma 9.4
1994 age-related hearing loss 9.4
1995 atrial fibrillation and stroke 9.4
1996 central cord syndrome 9.4
1997 cerebral arteriosclerosis 9.4
1998 cumulative trauma disorders 9.4
1999 hemifacial spasm 9.4
2000 myoclonus 9.4
2001 overuse syndrome 9.4
2002 repetitive motion disorders 9.4
2003 spasticity 9.4
2004 audiogenic seizures 9.4
2005 idiopathic central precocious puberty 9.4
2006 cleft lip with or without cleft palate 9.4
2007 primary peritoneal carcinoma 9.4
2008 mixed germ cell tumor 9.4
2009 genetic neuromuscular disease 9.4
2010 differentiated thyroid carcinoma 9.4
2011 systemic autoimmune disease 9.4
2012 adrenogenital syndrome 9.4
2013 orofacial clefting syndrome 9.4
2014 genetic hypertension 9.4
2015 immune complex mediated vasculitis 9.4
2016 low-grade astrocytoma 9.4
2017 papillary tumor of the pineal region 9.4
2018 uniparental disomy of chromosome 14 9.4
2019 cerebral sinovenous thrombosis 9.4
2020 idiopathic nephrotic syndrome 9.4
2021 obsolete: brachydactyly of fingers 9.4
2022 familial intrahepatic cholestasis 9.4
2023 acyl-coa dehydrogenase deficiency 9.4
2024 homozygous familial hypercholesterolemia 9.4
2025 idiopathic avascular necrosis 9.4
2026 osteonecrosis of the jaw 9.4
2027 necrotizing soft tissue infection 9.4
2028 primitive portal vein thrombosis 9.4
2029 secondary sclerosing cholangitis 9.4
2030 semicircular canal dehiscence syndrome 9.4
2031 ankylostomiasis 9.4
2032 pattern dystrophy 9.4
2033 argyria 9.4
2034 disorder of energy metabolism 9.4
2035 rasopathy 9.4
2036 rare intellectual disability 9.4
2037 primary lipodystrophy 9.4
2038 other metabolic disease 9.4
2039 non-functioning pituitary adenoma 9.4
2040 microtia 9.4
2041 lumbar syndrome 9.4
2042 autosomal trisomy 9.4
2043 paternal uniparental disomy 9.4
2044 polyploidy 9.4
2045 severe immune-mediated enteropathy 9.4
2046 secondary glomerular disease 9.4
2047 basement membrane disease 9.4
2048 acute motor axonal neuropathy 9.4
2049 multiple system atrophy, parkinsonian type 9.4
2050 colobomatous microphthalmia 9.4
2051 acquired lipodystrophy 9.4
2052 intestinal polyposis syndrome 9.4
2053 undetermined colitis 9.4
2054 multiple congenital anomalies/dysmorphic syndrome-intellectual disability 9.4
2055 primary glomerular disease 9.4
2056 polyendocrinopathy 9.4
2057 neurogenic thoracic outlet syndrome 9.4
2058 cutaneous myiasis 9.4
2059 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 1224, show less)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1
Oseltamivir Approved Phase 4 204255-11-8, 196618-13-0 65028
2
Citalopram Approved Phase 4 59729-33-8 2771
3
Erythromycin Approved, Investigational, Vet_approved Phase 4 114-07-8 441411 12560
4
Vancomycin Approved Phase 4 1404-90-6 441141 14969
5
Lixisenatide Approved Phase 4 320367-13-3
6
Ceftaroline fosamil Approved, Investigational Phase 4 229016-73-3
7
Metyrapone Approved, Investigational Phase 4 54-36-4 4174