BMIQ12
MCID: BDY015
MIFTS: 32

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 58 30 6 41
Obesity, Susceptibility to, Bmiq12 58 13
Obesity 58 74
Obesity, Susceptibility to 58
Obesity Bmiq12 58
Bmiq12 58

Classifications:



External Ids:

OMIM 58 612362
UMLS 74 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). Affiliated tissues include bone, heart and liver.

Description 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 1230, show less)
# Related Disease Score Top Affiliating Genes
1 proprotein convertase 1/3 deficiency 32.2 LOC101929710 PCSK1
2 body mass index quantitative trait locus 11 12.6
3 obesity, early-onset, with adrenal insufficiency and red hair 12.6
4 morbid obesity and spermatogenic failure 12.5
5 obesity-hypoventilation syndrome 12.4
6 mental retardation, truncal obesity, retinal dystrophy, and micropenis syndrome 12.4
7 obesity, hyperphagia, and developmental delay 12.4
8 abdominal obesity-metabolic syndrome 1 12.4
9 spastic paraplegia, intellectual disability, nystagmus, and obesity 12.4
10 retinal dystrophy and obesity 12.4
11 abdominal obesity-metabolic syndrome 3 12.4
12 leptin deficiency or dysfunction 12.4
13 wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome 12.4
14 developmental delay, intellectual disability, obesity, and dysmorphic features 12.4
15 hypothalamic obesity 12.3
16 x-linked intellectual disability - short stature - obesity 12.3
17 obesity due to congenital leptin deficiency 12.3
18 aniridia - ptosis - intellectual disability - familial obesity 12.2
19 abdominal obesity-metabolic syndrome quantitative trait locus 2 12.2
20 leptin receptor deficiency 12.2
21 hydrocephalus obesity hypogonadism 12.2
22 intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity 12.2
23 rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome 12.1
24 obesity due to congenital leptin resistance 12.1
25 severe early-onset obesity-insulin resistance syndrome due to sh2b1 deficiency 12.1
26 obesity due to sim1 deficiency 12.1
27 body mass index quantitative trait locus 19 12.1
28 wilson-turner x-linked mental retardation syndrome 12.1
29 midface hypoplasia, obesity, developmental delay, and neonatal hypotonia 12.1
30 coloboma-obesity-hypogenitalism-mental retardation syndrome 12.0
31 cohen syndrome 12.0
32 prolactin deficiency with obesity and enlarged testes 12.0
33 short stature-obesity syndrome 12.0
34 mental retardation, obesity, mandibular prognathism, and eye and skin anomalies 12.0
35 genetic non-syndromic obesity 12.0
36 congenital leptin deficiency 11.9
37 momo syndrome 11.9
38 x-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome 11.9
39 intellectual disability-seizures-macrocephaly-obesity syndrome 11.9
40 intellectual disability-obesity-brain malformations-facial dysmorphism syndrome 11.9
41 obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome 11.9
42 ayazi syndrome 11.8
43 body mass index quantitative trait locus 18 11.8
44 body mass index quantitative trait locus 8 11.8
45 body mass index quantitative trait locus 7 11.8
46 body mass index quantitative trait locus 14 11.8
47 rohhad 11.8
48 mehmo syndrome 11.8
49 body mass index quantitative trait locus 10 11.8
50 body mass index quantitative trait locus 20 11.8
51 chops syndrome 11.7
52 coenzyme q10 deficiency, primary, 2 11.7
53 hyperostosis frontalis interna 11.6
54 body mass index quantitative trait locus 9 11.6
55 body mass index quantitative trait locus 4 11.6
56 diabetes mellitus, noninsulin-dependent 11.6
57 prader-willi syndrome 11.6
58 man1b1-cdg 11.5
59 fatty liver disease 11.5
60 polycystic ovary syndrome 11.5
61 diploid-triploid mosaicism 11.5
62 glucose intolerance 11.4
63 carpenter syndrome 1 11.4
64 bardet-biedl syndrome 12 11.4
65 alstrom syndrome 11.4
66 bardet-biedl syndrome 1 11.4
67 borjeson-forssman-lehmann syndrome 11.4
68 conn's syndrome 11.4
69 bardet-biedl syndrome 11.4
70 bardet-biedl syndrome 2 11.4
71 eating disorder 11.4
72 sleep apnea 11.3
73 bardet-biedl syndrome 4 11.3
74 pseudopseudohypoparathyroidism 11.3
75 fatty liver disease, nonalcoholic 1 11.3
76 gallbladder disease 1 11.3
77 bardet-biedl syndrome 10 11.3
78 bardet-biedl syndrome 11 11.3
79 breast cancer 11.3
80 nonalcoholic steatohepatitis 11.3
81 diabetes mellitus, ketosis-prone 11.3
82 pituitary adenoma 4, acth-secreting 11.3
83 bardet-biedl syndrome 6 11.3
84 albright's hereditary osteodystrophy 11.2
85 prediabetes syndrome 11.2
86 mental retardation, autosomal dominant 39 11.2
87 hypertriglyceridemia, familial 11.2
88 acanthosis nigricans 11.2
89 biemond syndrome ii 11.2
90 hepatocellular carcinoma 11.2
91 vascular disease 11.2
92 pulmonary embolism 11.2
93 renal cell carcinoma, nonpapillary 11.2
94 hernia, hiatus 11.2
95 neural tube defects 11.2
96 migraine with or without aura 1 11.2
97 focal segmental glomerulosclerosis 11.1
98 stroke, ischemic 11.1
99 esophageal cancer 11.1
100 laron syndrome 11.1
101 myeloma, multiple 11.1
102 blount's disease 11.1
103 varicose veins 11.1
104 achondroplasia 11.1
105 schaaf-yang syndrome 11.1
106 monogenic diabetes 11.1
107 hypersomnia 11.1
108 mental retardation, x-linked, syndromic, cabezas type 11.1
109 coronary artery disease, autosomal dominant, 1 11.1
110 empty sella syndrome 11.1
111 acth-secreting pituitary adenoma 11.1
112 biemond syndrome 11.1
113 classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 11.1
114 idiopathic edema 11.1
115 bardet-biedl syndrome 3 11.1
116 chromosome 16p11.2 deletion syndrome, 220-kb 11.1
117 adiposis dolorosa 11.0
118 pseudohypoparathyroidism, type ia 11.0
119 ulnar-mammary syndrome 11.0
120 pseudohypoparathyroidism, type ic 11.0
121 acrodysostosis 1 with or without hormone resistance 10.9
122 chromosome 16p12.1 deletion syndrome, 520-kb 10.9
123 growth hormone insensitivity with immunodeficiency 10.9
124 prader-willi habitus, osteopenia, and camptodactyly 10.9
125 aromatase deficiency 10.9
126 chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb 10.9
127 carpenter syndrome 2 10.9
128 pigmented nodular adrenocortical disease, primary, 4 10.9
129 bardet-biedl syndrome 5 10.9
130 bardet-biedl syndrome 7 10.9
131 bardet-biedl syndrome 8 10.9
132 bardet-biedl syndrome 9 10.9
133 bardet-biedl syndrome 13 10.9
134 bardet-biedl syndrome 14 10.9
135 bardet-biedl syndrome 16 10.9
136 bardet-biedl syndrome 17 10.9
137 bardet-biedl syndrome 18 10.9
138 bardet-biedl syndrome 19 10.9
139 bardet-biedl syndrome 20 10.9
140 bardet-biedl syndrome 21 10.9
141 kleefstra syndrome 10.9
142 pelvic lipomatosis 10.9
143 clark-baraitser syndrome 10.9
144 camera-marugo-cohen syndrome 10.9
145 short stature, brachydactyly, intellectual developmental disability, and seizures 10.9
146 diabetes mellitus 10.9
147 liver disease 10.8
148 nonalcoholic fatty liver disease 10.8
149 pituitary adenoma 1, multiple types 10.8
150 maturity-onset diabetes of the young, type 2 10.8
151 hepatitis b vaccine, response to 10.8
152 precocious puberty, central, 1 10.8
153 rubinstein-taybi syndrome 1 10.8
154 polycystic ovary syndrome 1 10.8
155 acth-independent macronodular adrenal hyperplasia 10.8
156 mental retardation, x-linked, syndromic, nascimento type 10.8
157 chromosome xq27.3-q28 duplication syndrome 10.8
158 diabetes mellitus, noninsulin-dependent, 1 10.8
159 renal cell carcinoma, papillary, 1 10.8
160 high density lipoprotein cholesterol level quantitative trait locus 1 10.8
161 lipodystrophy, familial partial, type 1 10.8
162 pigmented nodular adrenocortical disease, primary, 2 10.8
163 pigmented nodular adrenocortical disease, primary, 1 10.8
164 neutral lipid storage disease with myopathy 10.8
165 pigmented nodular adrenocortical disease, primary, 3 10.8
166 precocious puberty, central, 2 10.8
167 acth-independent macronodular adrenal hyperplasia 2 10.8
168 bardet-biedl syndrome 15 10.8
169 diabetes mellitus, noninsulin-dependent, 5 10.8
170 temple syndrome 10.8
171 senior-loken syndrome 9 10.8
172 luscan-lumish syndrome 10.8
173 primary pigmented nodular adrenocortical disease 10.8
174 chromosome 15q24 deletion syndrome 10.8
175 syndromic x-linked intellectual disability 7 10.8
176 syndromic x-linked intellectual disability shashi type 10.8
177 cortisone reductase deficiency 10.8
178 rickets 10.8
179 bell's palsy 10.8
180 carcinosarcoma 10.8
181 froelich syndrome 10.8
182 2q37 deletion syndrome 10.8
183 48,xxyy syndrome 10.8
184 cerebro-oculo-facio-skeletal syndrome 10.8
185 cockayne syndrome type ii 10.8
186 hernández-aguirre negrete syndrome 10.8
187 hyperadrenalism 10.8
188 lipodermatosclerosis 10.8
189 localized lipodystrophy 10.8
190 macular telangiectasia type 2 10.8
191 male pseudohermaphroditism intellectual disability syndrome, verloes type 10.8
192 mthfr gene variant 10.8
193 proximal chromosome 18q deletion syndrome 10.8
194 septo-optic dysplasia spectrum 10.8
195 body mass index quantitative trait locus 1 10.7
196 hyperinsulinism 10.7
197 degos 'en cocarde' erythrokeratoderma 10.6
198 lipid metabolism disorder 10.6
199 asthma 10.6
200 gestational diabetes 10.6
201 depression 10.5
202 hyperglycemia 10.5
203 endometrial cancer 10.5
204 heart disease 10.5
205 lipedema 10.5
206 fish-eye disease 10.5
207 hypertension, essential 10.5
208 gastroesophageal reflux 10.5
209 kidney disease 10.5
210 osteoarthritis 10.4
211 apnea, obstructive sleep 10.4
212 rere-related disorders 10.4
213 hypogonadism 10.4
214 hypogonadotropism 10.4
215 aging 10.4
216 chronic kidney failure 10.4
217 coronary heart disease 1 10.4
218 periodontitis 10.4
219 arteries, anomalies of 10.4
220 anorexia nervosa 10.3
221 thyroiditis 10.3
222 coronary artery anomaly 10.3
223 colorectal cancer 10.3
224 arthritis 10.3
225 prostate cancer 10.3
226 prostate cancer, hereditary, 8 10.3
227 prostate cancer, hereditary, 6 10.3
228 anxiety 10.3
229 lymphomatous thyroiditis 10.3
230 dental caries 10.3
231 cystadenoma 10.3
232 myocardial infarction 10.3
233 adenocarcinoma 10.3
234 craniopharyngioma 10.3
235 infertility 10.3
236 neuropathy 10.3
237 leukemia 10.3
238 pancreatitis 10.3
239 hypoxia 10.3
240 periodontal disease 10.3
241 hyperandrogenism 10.3
242 alacrima, achalasia, and mental retardation syndrome 10.3
243 insulin-like growth factor i 10.3
244 spondyloocular syndrome 10.3
245 muscle hypertrophy 10.3
246 psoriasis 10.2
247 pre-eclampsia 10.2
248 hepatitis 10.2
249 hypothyroidism 10.2
250 intracranial hypertension 10.2
251 impotence 10.2
252 hyperuricemia 10.2
253 acute pancreatitis 10.2
254 rheumatoid arthritis 10.2
255 osteoporosis 10.2
256 breast reconstruction 10.2
257 thrombosis 10.2
258 ischemia 10.2
259 atherosclerosis susceptibility 10.2
260 iron metabolism disease 10.2
261 lymphedema 10.2
262 disease of mental health 10.2
263 pancreatic cancer 10.2
264 barrett esophagus 10.2
265 congestive heart failure 10.2
266 overnutrition 10.2
267 leukemia, acute lymphoblastic 10.2
268 lymphocytic leukemia 10.2
269 attention deficit-hyperactivity disorder 10.2
270 down syndrome 10.2
271 pol iii-related leukodystrophies 10.2
272 adenoma 10.2
273 hypoglycemia 10.2
274 schizophrenia 10.2
275 lymphoma 10.2
276 atrial fibrillation 10.2
277 respiratory failure 10.2
278 alzheimer disease 10.1
279 bipolar disorder 10.1
280 periodontitis, chronic 10.1
281 inflammatory bowel disease 10.1
282 influenza 10.1
283 esophagitis 10.1
284 hepatitis c 10.1
285 laryngeal adductor paralysis 10.1
286 autism 10.1
287 bulimia nervosa 10.1
288 pulmonary hypertension 10.1
289 acute myocardial infarction 10.1
290 ischemic heart disease 10.1
291 sexual disorder 10.1
292 thyroid cancer 10.1
293 lipomatosis 10.1
294 peripheral nervous system disease 10.1
295 ovarian cancer 10.1
296 gastric cancer 10.1
297 spinal cord injury 10.1
298 cytokine deficiency 10.1
299 multiple sclerosis 10.1
300 intracranial hypertension, idiopathic 10.1
301 neutrophil actin dysfunction 10.1
302 prostatic hyperplasia, benign 10.1
303 pulmonary disease, chronic obstructive 10.1
304 ovarian disease 10.1
305 prostatic adenoma 10.1
306 precocious puberty 10.1
307 hypervitaminosis a 10.1
308 carotenemia 10.1
309 hypervitaminosis d 10.1
310 horns in sheep 10.1
311 major depressive disorder 10.1
312 nephrolithiasis 10.1
313 hyperparathyroidism 10.1
314 bowenoid papulosis 10.1
315 frontal fibrosing alopecia 10.1
316 atrial standstill 1 10.1
317 microvascular complications of diabetes 3 10.1
318 microvascular complications of diabetes 4 10.1
319 microvascular complications of diabetes 5 10.1
320 microvascular complications of diabetes 6 10.1
321 microvascular complications of diabetes 7 10.1
322 liver cirrhosis 10.1
323 rectum cancer 10.1
324 fibromyalgia 10.1
325 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 10.1
326 peripheral vascular disease 10.1
327 mood disorder 10.1
328 pustulosis of palm and sole 10.1
329 acute respiratory distress syndrome 10.1
330 ige responsiveness, atopic 10.0
331 bone mineral density quantitative trait locus 8 10.0
332 bone mineral density quantitative trait locus 15 10.0
333 end stage renal failure 10.0
334 colitis 10.0
335 gallbladder disease 10.0
336 hypogonadotropic hypogonadism 10.0
337 kidney cancer 10.0
338 appendicitis 10.0
339 pain - chronic 10.0
340 encephalopathy 10.0
341 psoriatic arthritis 10.0
342 dermatitis 10.0
343 situs inversus 10.0
344 placenta disease 10.0
345 growth hormone deficiency 10.0
346 headache 10.0
347 blood group, colton system 10.0
348 acute lymphocytic leukemia 10.0
349 alexithymia 10.0
350 eclampsia 10.0
351 wernicke encephalopathy 10.0
352 irritable bowel syndrome 10.0
353 alcohol dependence 10.0
354 sjogren syndrome 10.0
355 helicobacter pylori infection 10.0
356 male infertility 10.0
357 autism spectrum disorder 10.0
358 secondary hyperparathyroidism 10.0
359 gout 10.0
360 mental depression 10.0
361 aortic aneurysm 10.0
362 rhinitis 10.0
363 pneumonia 10.0
364 lung disease 10.0
365 hypotonia 10.0
366 thrombophilia due to thrombin defect 10.0
367 acute lymphoblastic leukemia, childhood 10.0
368 cerebral palsy 10.0
369 colorectal adenoma 10.0
370 crohn's disease 10.0
371 insulinoma 10.0
372 cholelithiasis 10.0
373 dementia 10.0
374 diverticulitis 10.0
375 narcolepsy 10.0
376 achalasia 10.0
377 rapidly involuting congenital hemangioma 10.0
378 aortic aneurysm, familial abdominal, 1 10.0
379 celiac disease 1 10.0
380 nance-horan syndrome 10.0
381 dermatitis, atopic 10.0
382 allergic rhinitis 10.0
383 deficiency anemia 10.0
384 cataract 10.0
385 severe combined immunodeficiency 10.0
386 melanoma 10.0
387 pseudohypoparathyroidism 10.0
388 combined t cell and b cell immunodeficiency 10.0
389 focal segmental glomerulosclerosis 1 10.0
390 global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 10.0
391 bone disease 10.0
392 human immunodeficiency virus infectious disease 10.0
393 lupus erythematosus 10.0
394 systolic heart failure 10.0
395 dextrocardia with situs inversus 10.0
396 ovarian epithelial cancer 10.0
397 slipped capital femoral epiphysis 10.0
398 epiphysiolysis of the hip 10.0
399 systemic lupus erythematosus 9.9
400 lymphoma, hodgkin, classic 9.9
401 hypopituitarism 9.9
402 fetal macrosomia 9.9
403 neurofibromatosis, type ii 9.9
404 aplasia cutis congenita, nonsyndromic 9.9
405 autoimmune disease 9.9
406 cardiac conduction defect 9.9
407 carpal tunnel syndrome 9.9
408 intussusception 9.9
409 pulmonary hypertension, primary, 1 9.9
410 lung cancer 9.9
411 acute insulin response 9.9
412 lymphoma, non-hodgkin, familial 9.9
413 mononeuropathy of the median nerve, mild 9.9
414 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.9
415 thrombocytopenia 9.9
416 endometrial hyperplasia 9.9
417 autonomic neuropathy 9.9
418 infant gynecomastia 9.9
419 goiter 9.9
420 gynecomastia 9.9
421 acute cystitis 9.9
422 polyneuropathy 9.9
423 personality disorder 9.9
424 epilepsy 9.9
425 learning disability 9.9
426 osteoporotic fracture 9.9
427 otitis media 9.9
428 tetralogy of fallot 9.9
429 neural tube defects, folate-sensitive 9.9
430 cervical cancer 9.9
431 burns 9.9
432 fecal incontinence 9.9
433 pain agnosia 9.9
434 sialadenitis 9.9
435 sarcoma 9.9
436 gastroparesis 9.9
437 arteriosclerosis 9.9
438 iga glomerulonephritis 9.9
439 thoracic outlet syndrome 9.9
440 clear cell renal cell carcinoma 9.9
441 elephantiasis 9.9
442 dwarfism 9.9
443 pelvic organ prolapse 9.9
444 hemochromatosis, type 1 9.9
445 polydactyly 9.9
446 salla disease 9.9
447 maturity-onset diabetes of the young 9.9
448 meningioma, familial 9.9
449 resting heart rate, variation in 9.9
450 infantile liver failure syndrome 1 9.9
451 hepatitis b 9.9
452 angiosarcoma 9.9
453 restless legs syndrome 9.9
454 peripheral artery disease 9.9
455 hepatocellular adenoma 9.9
456 scoliosis 9.9
457 obstructive nephropathy 9.9
458 spinal meningioma 9.9
459 hidradenitis suppurativa 9.9
460 retinitis 9.9
461 secretory meningioma 9.9
462 pituitary gland disease 9.9
463 paraplegia 9.9
464 cerebrovascular disease 9.9
465 polycythemia 9.9
466 retinal degeneration 9.9
467 developmental coordination disorder 9.9
468 juvenile hereditary hemochromatosis 9.9
469 heparin-induced thrombocytopenia 9.9
470 developmental dyspraxia 9.9
471 bladder cancer 9.8
472 sarcoidosis 1 9.8
473 lipoid congenital adrenal hyperplasia 9.8
474 cryptorchidism, unilateral or bilateral 9.8
475 hypogonadism, male 9.8
476 retinitis pigmentosa 9.8
477 macular degeneration, age-related, 1 9.8
478 homocysteinemia 9.8
479 leber congenital amaurosis 4 9.8
480 autoimmune disease 1 9.8
481 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 9.8
482 alcohol abuse 9.8
483 dilated cardiomyopathy 9.8
484 pemphigus foliaceus 9.8
485 skin disease 9.8
486 limb ischemia 9.8
487 venous insufficiency 9.8
488 iron deficiency anemia 9.8
489 amenorrhea 9.8
490 constipation 9.8
491 hidradenitis 9.8
492 retinal vascular disease 9.8
493 anovulation 9.8
494 gastritis 9.8
495 schizoaffective disorder 9.8
496 peritonitis 9.8
497 amyloidosis 9.8
498 allergic asthma 9.8
499 muscular dystrophy 9.8
500 acute mountain sickness 9.8
501 central precocious puberty 9.8
502 spondyloarthropathy 1 9.8
503 hypercarotenemia and vitamin a deficiency, autosomal dominant 9.8
504 nephrolithiasis, calcium oxalate 9.8
505 retinoblastoma 9.8
506 smith-magenis syndrome 9.8
507 spondylolisthesis 9.8
508 wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 9.8
509 diabetes mellitus, insulin-dependent 9.8
510 3-hydroxyacyl-coa dehydrogenase deficiency 9.8
511 phenylketonuria 9.8
512 mend syndrome 9.8
513 leukemia, acute myeloid 9.8
514 gastrointestinal stromal tumor 9.8
515 aspirin resistance 9.8
516 blood group, junior system 9.8
517 hyperprolactinemia 9.8
518 nevus comedonicus 9.8
519 angina pectoris 9.8
520 acute leukemia 9.8
521 joint disorders 9.8
522 pancreas adenocarcinoma 9.8
523 ulcerative colitis 9.8
524 idiopathic scoliosis 9.8
525 cardiac arrest 9.8
526 myelomeningocele 9.8
527 bone resorption disease 9.8
528 sensorineural hearing loss 9.8
529 bacterial infectious disease 9.8
530 microinvasive gastric cancer 9.8
531 chlamydia 9.8
532 keratomalacia 9.8
533 pulmonary edema 9.8
534 portal vein thrombosis 9.8
535 beriberi 9.8
536 peptic esophagitis 9.8
537 panniculitis 9.8
538 hyperostosis 9.8
539 papilloma 9.8
540 substance abuse 9.8
541 gingivitis 9.8
542 skin carcinoma 9.8
543 turner syndrome 9.8
544 scrapie 9.8
545 lymphopenia 9.8
546 spondylitis 9.8
547 fundus dystrophy 9.8
548 myeloid leukemia 9.8
549 exophthalmos 9.8
550 diabetes insipidus 9.8
551 hypertrophic cardiomyopathy 9.8
552 allergic encephalomyelitis 9.8
553 chromosomal triplication 9.8
554 soft tissue sarcoma 9.8
555 cardiogenic shock 9.8
556 hyperlipidemia, familial combined 9.7
557 lipomatosis, multiple symmetric 9.7
558 lipomatosis, multiple 9.7
559 pheochromocytoma 9.7
560 pilonidal sinus 9.7
561 pulmonary alveolar microlithiasis 9.7
562 scapuloperoneal myopathy, x-linked dominant 9.7
563 bornholm eye disease 9.7
564 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 9.7
565 taqi polymorphism 9.7
566 yemenite deaf-blind hypopigmentation syndrome 9.7
567 cholangiocarcinoma 9.7
568 helix syndrome 9.7
569 tendinopathy 9.7
570 tendinitis 9.7
571 bone fracture 9.7
572 glomerulonephritis 9.7
573 glycogen storage disease 9.7
574 neutropenia 9.7
575 spinal stenosis 9.7
576 chlamydia pneumonia 9.7
577 congenital hypothyroidism 9.7
578 adrenal gland pheochromocytoma 9.7
579 inguinal hernia 9.7
580 pleomorphic lipoma 9.7
581 primary hyperparathyroidism 9.7
582 allergic hypersensitivity disease 9.7
583 diarrhea 9.7
584 hyperinsulinemic hypoglycemia 9.7
585 bipolar i disorder 9.7
586 rheumatic disease 9.7
587 duodenal ulcer 9.7
588 viral hepatitis 9.7
589 dyspepsia 9.7
590 acromegaly 9.7
591 thrombophilia 9.7
592 endometrial adenocarcinoma 9.7
593 cellulitis 9.7
594 gastric adenocarcinoma 9.7
595 arthropathy 9.7
596 spindle cell sarcoma 9.7
597 coronary stenosis 9.7
598 monoclonal gammopathy of uncertain significance 9.7
599 muscular atrophy 9.7
600 hyperthyroidism 9.7
601 intestinal volvulus 9.7
602 dyskinesia of esophagus 9.7
603 cholangitis 9.7
604 postpartum depression 9.7
605 hypereosinophilic syndrome 9.7
606 amyloidosis aa 9.7
607 xp22.3 microdeletion syndrome 9.7
608 cryptogenic cirrhosis 9.7
609 cerebral beriberi 9.7
610 coffin-siris syndrome 1 9.7
611 hashimoto thyroiditis 9.7
612 kaposi sarcoma 9.7
613 carney complex, type 1 9.7
614 scoliosis, isolated 1 9.7
615 cystic fibrosis 9.7
616 myasthenia gravis 9.7
617 graves disease 1 9.7
618 caronte 9.7
619 mycobacterium tuberculosis 1 9.7
620 myopathy, myosin storage, autosomal dominant 9.7
621 human immunodeficiency virus type 1 9.7
622 malaria 9.7
623 intraocular pressure quantitative trait locus 9.7
624 myelodysplastic syndrome 9.7
625 graft-versus-host disease 9.7
626 aortic valve disease 2 9.7
627 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 9.7
628 blood group, gerbich system 9.7
629 baker-gordon syndrome 9.7
630 arteriovenous fistula 9.7
631 critical limb ischemia 9.7
632 degenerative disc disease 9.7
633 hematopoietic stem cell transplantation 9.7
634 intermittent claudication 9.7
635 keratoconus 9.7
636 pancreatic ductal adenocarcinoma 9.7
637 pulmonary emphysema 9.7
638 familial partial lipodystrophy 9.7
639 chronic venous insufficiency 9.7
640 estrogen-receptor positive breast cancer 9.7
641 umbilical hernia 9.7
642 ectopic pregnancy 9.7
643 osteomalacia 9.7
644 japanese encephalitis 9.7
645 multiple personality disorder 9.7
646 hydronephrosis 9.7
647 t cell deficiency 9.7
648 autonomic nervous system disease 9.7
649 nephrotic syndrome 9.7
650 patulous eustachian tube 9.7
651 kwashiorkor 9.7
652 cholestasis 9.7
653 papilledema 9.7
654 squamous cell carcinoma 9.7
655 post-thrombotic syndrome 9.7
656 gastric dilatation 9.7
657 purpura 9.7
658 liposarcoma 9.7
659 breast disease 9.7
660 plague 9.7
661 duodenal obstruction 9.7
662 lactic acidosis 9.7
663 pituitary adenoma 9.7
664 glucose metabolism disease 9.7
665 calciphylaxis 9.7
666 intrahepatic cholangiocarcinoma 9.7
667 neurotic disorder 9.7
668 ovarian cyst 9.7
669 sleep disorder 9.7
670 gastric cardia adenocarcinoma 9.7
671 peptic ulcer disease 9.7
672 gastrointestinal system disease 9.7
673 night blindness 9.7
674 vasculitis 9.7
675 eosinophilia-myalgia syndrome 9.7
676 microcephaly 9.7
677 aortic coarctation 9.7
678 brain tumor, childhood 9.7
679 fournier gangrene 9.7
680 glioma 9.7
681 myasthenia gravis congenital 9.7
682 pediatric hypertension 9.7
683 polymyositis 9.7
684 clopidogrel resistance 9.7
685 syncope 9.7
686 dysphagia 9.7
687 xq12-q13.3 duplication syndrome 9.7
688 cerebral amyloid angiopathy, cst3-related 9.6
689 angelman syndrome 9.6
690 holt-oram syndrome 9.6
691 optic nerve hypoplasia, bilateral 9.6
692 small cell cancer of the lung 9.6
693 thyroid cancer, nonmedullary, 1 9.6
694 tobacco addiction 9.6
695 williams-beuren syndrome 9.6
696 adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency 9.6
697 ascites, chylous 9.6
698 disorganization, mouse, homolog of 9.6
699 galactorrhea 9.6
700 mckusick-kaufman syndrome 9.6
701 myxedema 9.6
702 lysosomal acid lipase deficiency 9.6
703 arts syndrome 9.6
704 muscular dystrophy, duchenne type 9.6
705 pituitary adenoma, prolactin-secreting 9.6
706 ventricular fibrillation, paroxysmal familial, 1 9.6
707 sickle cell anemia 9.6
708 huntington disease-like 2 9.6
709 leukemia, chronic myeloid 9.6
710 prostate cancer, hereditary, 7 9.6
711 preterm premature rupture of the membranes 9.6
712 deafness-infertility syndrome 9.6
713 bestrophinopathy, autosomal recessive 9.6
714 adiponectin, serum level of, quantitative trait locus 1 9.6
715 plasminogen activator inhibitor-1 deficiency 9.6
716 hemorrhage, intracerebral 9.6
717 peripartum cardiomyopathy 9.6
718 hyperproinsulinemia 9.6
719 fetal akinesia deformation sequence 2 9.6
720 alopecia 9.6
721 anal fistula 9.6
722 brain injury 9.6
723 bronchopulmonary dysplasia 9.6
724 cerebral hemorrhage 9.6
725 diabetic neuropathy 9.6
726 diffuse large b-cell lymphoma 9.6
727 hydrocephalus 9.6
728 osteochondrosis 9.6
729 renal tubular acidosis 9.6
730 dengue shock syndrome 9.6
731 vitamin b12 deficiency 9.6
732 metabolic acidosis 9.6
733 androgenic alopecia 9.6
734 colorectal adenocarcinoma 9.6
735 crohn's colitis 9.6
736 ptosis 9.6
737 steatorrhea 9.6
738 short bowel syndrome 9.6
739 open-angle glaucoma 9.6
740 portal hypertension 9.6
741 thrombotic thrombocytopenic purpura 9.6
742 borderline personality disorder 9.6
743 hypertensive heart disease 9.6
744 cauda equina syndrome 9.6
745 penile cancer 9.6
746 lyme disease 9.6
747 protein-energy malnutrition 9.6
748 hemosiderosis 9.6
749 pica disease 9.6
750 chagas disease 9.6
751 pathological gambling 9.6
752 carotid stenosis 9.6
753 severe pre-eclampsia 9.6
754 megaesophagus 9.6
755 diabetic cataract 9.6
756 megaloblastic anemia 9.6
757 azoospermia 9.6
758 dumping syndrome 9.6
759 cholera 9.6
760 urticaria 9.6
761 calcinosis 9.6
762 rectum adenocarcinoma 9.6
763 post-traumatic stress disorder 9.6
764 colon adenocarcinoma 9.6
765 synovitis 9.6
766 endometriosis 9.6
767 cystic kidney disease 9.6
768 antiphospholipid syndrome 9.6
769 astrocytoma 9.6
770 interstitial lung disease 9.6
771 gallbladder cancer 9.6
772 tracheal stenosis 9.6
773 teratoma 9.6
774 hypertrichosis 9.6
775 pyoderma 9.6
776 myopathy 9.6
777 neuromuscular disease 9.6
778 prostate disease 9.6
779 urinary tract obstruction 9.6
780 bronchitis 9.6
781 inflammatory breast carcinoma 9.6
782 juvenile rheumatoid arthritis 9.6
783 compartment syndrome 9.6
784 mediastinitis 9.6
785 myocarditis 9.6
786 chronic fatigue syndrome 9.6
787 vascular dementia 9.6
788 skin melanoma 9.6
789 central sleep apnea 9.6
790 cleft lip 9.6
791 dacryoadenitis 9.6
792 fasciitis 9.6
793 plantar fasciitis 9.6
794 diastolic heart failure 9.6
795 drug dependence 9.6
796 hemophilia 9.6
797 myotonic dystrophy 9.6
798 polycystic kidney disease 9.6
799 acute graft versus host disease 9.6
800 cervical intraepithelial neoplasia 9.6
801 glucagonoma 9.6
802 glyceraldehyde-3-phosphate dehydrogenase deficiency 9.6
803 meralgia paresthetica 9.6
804 myotonia atrophica 9.6
805 pediatric multiple sclerosis 9.6
806 sudden sensorineural hearing loss 9.6
807 tremor 9.6
808 cytomegalovirus infection 9.6
809 cleft lip/palate 9.6
810 pfeiffer syndrome 9.4
811 alzheimer disease 2 9.4
812 amyotrophic lateral sclerosis 1 9.4
813 arteriovenous malformations of the brain 9.4
814 alopecia, androgenetic, 1 9.4
815 blood group, langereis system 9.4
816 radin blood group antigen 9.4
817 brachydactyly-nystagmus-cerebellar ataxia 9.4
818 cardiac arrhythmia 9.4
819 cleft palate, isolated 9.4
820 coloboma of macula 9.4
821 earlobe crease 9.4
822 beckwith-wiedemann syndrome 9.4
823 multiple endocrine neoplasia, type i 9.4
824 camurati-engelmann disease 9.4
825 erythermalgia, primary 9.4
826 factor viii deficiency 9.4
827 frasier syndrome 9.4
828 lymphoma, mucosa-associated lymphoid type 9.4
829 glaucoma, primary open angle 9.4
830 goiter, multinodular 1, with or without sertoli-leydig cell tumors 9.4
831 developmental dysplasia of the hip 1 9.4
832 hypophosphatemic bone disease 9.4
833 legg-calve-perthes disease 9.4
834 lipodystrophy, familial partial, type 2 9.4
835 marfan syndrome 9.4
836 medulloblastoma 9.4
837 moebius syndrome 9.4
838 pancreas, dorsal, agenesis of 9.4
839 polydactyly, postaxial, type a1 9.4
840 pulmonary fibrosis, idiopathic 9.4
841 raynaud disease 9.4
842 spinocerebellar ataxia 2 9.4
843 cryohydrocytosis 9.4
844 temporal arteritis 9.4
845 thrombophilia due to activated protein c resistance 9.4
846 digeorge syndrome 9.4
847 tracheoesophageal fistula with or without esophageal atresia 9.4
848 triiodothyronine receptor auxiliary protein 9.4
849 cardiomyopathy, familial hypertrophic, 1 9.4
850 vesicoureteral reflux 1 9.4
851 wolf-hirschhorn syndrome 9.4
852 anencephaly 9.4
853 central hypoventilation syndrome, congenital 9.4
854 cardiomyopathy, dilated, with hypergonadotropic hypogonadism 9.4
855 joubert syndrome 1 9.4
856 cerebrotendinous xanthomatosis 9.4
857 chediak-higashi syndrome 9.4
858 craniosynostosis with fibular aplasia 9.4
859 mitochondrial complex iv deficiency 9.4
860 diastrophic dysplasia 9.4
861 fanconi anemia, complementation group a 9.4
862 halothane hepatitis 9.4
863 hydrocephalus, congenital, 1 9.4
864 hydrocephalus due to congenital stenosis of aqueduct of sylvius 9.4
865 hyperlipoproteinemia, type i 9.4
866 autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia 9.4
867 indifference to pain, congenital, autosomal recessive 9.4
868 cholestasis, benign recurrent intrahepatic, 1 9.4
869 lecithin:cholesterol acyltransferase deficiency 9.4
870 methane production 9.4
871 neuroblastoma 1 9.4
872 niemann-pick disease, type c1 9.4
873 ocular motor apraxia 9.4
874 raine syndrome 9.4
875 pituitary hormone deficiency, combined, 2 9.4
876 pycnodysostosis 9.4
877 inflammatory bowel disease 1 9.4
878 succinic semialdehyde dehydrogenase deficiency 9.4
879 werner syndrome 9.4
880 muscular dystrophy, becker type 9.4
881 fragile x syndrome 9.4
882 cornelia de lange syndrome 5 9.4
883 choroideremia 9.4
884 coffin-lowry syndrome 9.4
885 occipital horn syndrome 9.4
886 hemophilia a 9.4
887 mental retardation-hypotonic facies syndrome, x-linked, 1 9.4
888 emery-dreifuss muscular dystrophy 1, x-linked 9.4
889 androgen insensitivity, partial 9.4
890 frontotemporal dementia 9.4
891 tibial muscular dystrophy, tardive 9.4
892 abcd syndrome 9.4
893 fryns microphthalmia syndrome 9.4
894 mitochondrial import-stimulating factor 9.4
895 blood group--swann system 9.4
896 wilms tumor 5 9.4
897 papillary thyroid microcarcinoma 9.4
898 brittle bone disorder 9.4
899 intervertebral disc disease 9.4
900 aceruloplasminemia 9.4
901 rheumatoid arthritis, systemic juvenile 9.4
902 orthostatic intolerance 9.4
903 langerhans cell histiocytosis 9.4
904 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.4
905 anisomastia 9.4
906 narcolepsy 2 9.4
907 maturity-onset diabetes of the young, type 4 9.4
908 vitiligo-associated multiple autoimmune disease susceptibility 1 9.4
909 lipodystrophy, familial partial, type 7 9.4
910 bone mineral density quantitative trait locus 3 9.4
911 nasopharyngeal carcinoma 9.4
912 mammographic density 9.4
913 ichthyosis, cyclic, with epidermolytic hyperkeratosis 9.4
914 chromosome 1p36 deletion syndrome 9.4
915 ovarian cancer 1 9.4
916 ovarian hyperstimulation syndrome 9.4
917 platelet glycoprotein iv deficiency 9.4
918 carotid intimal medial thickness 2 9.4
919 ichthyosis prematurity syndrome 9.4
920 aplastic anemia 9.4
921 hepatitis c virus 9.4
922 testicular microlithiasis 9.4
923 asthma-related traits 4 9.4
924 cavitary optic disc anomalies 9.4
925 smoking as a quantitative trait locus 3 9.4
926 joubert syndrome 8 9.4
927 acute promyelocytic leukemia 9.4
928 alpha-1-antitrypsin deficiency 9.4
929 complement component 3 deficiency, autosomal recessive 9.4
930 protein z deficiency 9.4
931 aspergillosis 9.4
932 dengue virus 9.4
933 glycerol quantitative trait locus 9.4
934 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 9.4
935 hypobetalipoproteinemia, familial, 1 9.4
936 sacral agenesis with vertebral anomalies 9.4
937 glucocorticoid resistance, generalized 9.4
938 immunodeficiency 40 9.4
939 wilms tumor 6 9.4
940 hypertrophic scars 9.4
941 tendinosis 9.4
942 adult respiratory distress syndrome 9.4
943 alcoholic liver cirrhosis 9.4
944 aortic atherosclerosis 9.4
945 autoimmune hepatitis 9.4
946 b-cell lymphomas 9.4
947 bladder disease 9.4
948 craniosynostosis 9.4
949 emery-dreifuss muscular dystrophy, x-linked 9.4
950 exocrine pancreatic insufficiency 9.4
951 follicular lymphoma 9.4
952 gas gangrene 9.4
953 hemangioma 9.4
954 hemolytic anemia 9.4
955 holoprosencephaly 9.4
956 islet cell tumor 9.4
957 keloids 9.4
958 lymphoblastic lymphoma 9.4
959 muscle disorders 9.4
960 niemann-pick disease 9.4
961 osteochondritis dissecans 9.4
962 osteonecrosis 9.4
963 osteopetrosis 9.4
964 pulmonary fibrosis 9.4
965 severe congenital neutropenia 9.4
966 single ventricular heart 9.4
967 sinusitis 9.4
968 spinal muscular atrophy 9.4
969 temporal lobe epilepsy 9.4
970 traumatic brain injury 9.4
971 chikungunya 9.4
972 aspiration pneumonia 9.4
973 hypophosphatemia 9.4
974 multinodular goiter 9.4
975 brachydactyly 9.4
976 fetal alcohol syndrome 9.4
977 spastic cerebral palsy 9.4
978 female breast cancer 9.4
979 fetal alcohol spectrum disorder 9.4
980 chorioamnionitis 9.4
981 autosomal recessive disease 9.4
982 paraganglioma 9.4
983 zollinger-ellison syndrome 9.4
984 oral squamous cell carcinoma 9.4
985 pancreatic agenesis 9.4
986 colon adenoma 9.4
987 infective endocarditis 9.4
988 withdrawal disorder 9.4
989 janus kinase-3 deficiency 9.4
990 munchausen by proxy 9.4
991 ductal carcinoma in situ 9.4
992 estrogen-receptor negative breast cancer 9.4
993 ischemic colitis 9.4
994 microscopic colitis 9.4
995 ileitis 9.4
996 ileocolitis 9.4
997 stuttering 9.4
998 tracheomalacia 9.4
999 pollen allergy 9.4
1000 autoimmune neuropathy 9.4
1001 isolated growth hormone deficiency 9.4
1002 physical disorder 9.4
1003 mucositis 9.4
1004 superior semicircular canal dehiscence 9.4
1005 glycogen storage disease ixa 9.4
1006 migraine with aura 9.4
1007 pelvic inflammatory disease 9.4
1008 cysticercosis 9.4
1009 cerebral artery occlusion 9.4
1010 mumps 9.4
1011 endocarditis 9.4
1012 siderosis 9.4
1013 esophageal atresia 9.4
1014 gastric ulcer 9.4
1015 malignant hypertension 9.4
1016 voyeurism 9.4
1017 tethered spinal cord syndrome 9.4
1018 hypospadias 9.4
1019 depersonalization disorder 9.4
1020 myiasis 9.4
1021 henoch-schoenlein purpura 9.4
1022 prostatic hypertrophy 9.4
1023 pertussis 9.4
1024 spondyloarthropathy 9.4
1025 appendix cancer 9.4
1026 appendiceal neoplasm 9.4
1027 disseminated intravascular coagulation 9.4
1028 social phobia 9.4
1029 rabies 9.4
1030 diphtheria 9.4
1031 horner's syndrome 9.4
1032 diabetic autonomic neuropathy 9.4
1033 nephrosclerosis 9.4
1034 emery-dreifuss muscular dystrophy 9.4
1035 choledocholithiasis 9.4
1036 chronic laryngitis 9.4
1037 myopia 9.4
1038 pulmonary alveolar proteinosis 9.4
1039 lymphocytic choriomeningitis 9.4
1040 anisometropia 9.4
1041 paranoid schizophrenia 9.4
1042 varicocele 9.4
1043 entropion 9.4
1044 diabetic polyneuropathy 9.4
1045 guillain-barre syndrome 9.4
1046 choreatic disease 9.4
1047 conduct disorder 9.4
1048 vertebrobasilar insufficiency 9.4
1049 renal osteodystrophy 9.4
1050 mechanical entropion 9.4
1051 brain cancer 9.4
1052 coccidioidomycosis 9.4
1053 patent foramen ovale 9.4
1054 premature ejaculation 9.4
1055 plasmodium falciparum malaria 9.4
1056 familial lipoprotein lipase deficiency 9.4
1057 bacteriuria 9.4
1058 frozen shoulder 9.4
1059 sclerosing cholangitis 9.4
1060 leopard syndrome 9.4
1061 autosomal dominant cerebellar ataxia 9.4
1062 prostatitis 9.4
1063 hereditary angioedema 9.4
1064 angioedema 9.4
1065 thrombocytopenia due to platelet alloimmunization 9.4
1066 lymphadenitis 9.4
1067 benign breast phyllodes tumor 9.4
1068 neuroendocrine tumor 9.4
1069 ichthyosis 9.4
1070 histoplasmosis 9.4
1071 mitral valve stenosis 9.4
1072 factitious disorder 9.4
1073 hypothalamic disease 9.4
1074 cholecystitis 9.4
1075 enthesopathy 9.4
1076 heel spur 9.4
1077 tularemia 9.4
1078 granulomatous hepatitis 9.4
1079 lateral sclerosis 9.4
1080 agammaglobulinemia 9.4
1081 pancreas disease 9.4
1082 lymphangiosarcoma 9.4
1083 hemangioma of liver 9.4
1084 bilirubin metabolic disorder 9.4
1085 cranial nerve malignant neoplasm 9.4
1086 long qt syndrome 9.4
1087 laryngeal squamous cell carcinoma 9.4
1088 bronchiolitis 9.4
1089 acinar cell carcinoma 9.4
1090 mucinous adenocarcinoma 9.4
1091 food allergy 9.4
1092 anus disease 9.4
1093 complex regional pain syndrome 9.4
1094 bacterial vaginosis 9.4
1095 histiocytosis 9.4
1096 carotid artery disease 9.4
1097 laryngitis 9.4
1098 necrobiosis lipoidica 9.4
1099 mastocytosis 9.4
1100 superior mesenteric artery syndrome 9.4
1101 appendix adenocarcinoma 9.4
1102 mast cell neoplasm 9.4
1103 pleural empyema 9.4
1104 posterior cerebral artery infarction 9.4
1105 thrombophlebitis 9.4
1106 placental insufficiency 9.4
1107 mediastinal lipomatosis 9.4
1108 restrictive cardiomyopathy 9.4
1109 linitis plastica 9.4
1110 duodenogastric reflux 9.4
1111 microsporidiosis 9.4
1112 radiculopathy 9.4
1113 dyslexia 9.4
1114 extracutaneous mastocytoma 9.4
1115 uremia 9.4
1116 immune-complex glomerulonephritis 9.4
1117 trachea carcinoma 9.4
1118 alcoholic pancreatitis 9.4
1119 nutritional deficiency disease 9.4
1120 borna disease 9.4
1121 arteriolosclerosis 9.4
1122 aortic disease 9.4
1123 pulmonary coin lesion 9.4
1124 dystonia 9.4
1125 acute t cell leukemia 9.4
1126 large intestine cancer 9.4
1127 aortic valve insufficiency 9.4
1128 gastric liposarcoma 9.4
1129 ovarian serous cystadenocarcinoma 9.4
1130 adult lymphoma 9.4
1131 acquired immunodeficiency syndrome 9.4
1132 diffuse idiopathic skeletal hyperostosis 9.4
1133 peroneal nerve paralysis 9.4
1134 premenstrual tension 9.4
1135 peptic ulcer perforation 9.4
1136 parathyroid adenoma 9.4
1137 childhood leukemia 9.4
1138 cocaine abuse 9.4
1139 scabies 9.4
1140 complement component 3 deficiency 9.4
1141 actinomycosis 9.4
1142 mucormycosis 9.4
1143 acute cor pulmonale 9.4
1144 monocytic leukemia 9.4
1145 malignant hyperthermia 9.4
1146 pyoderma gangrenosum 9.4
1147 herpes simplex 9.4
1148 subacute delirium 9.4
1149 tongue cancer 9.4
1150 decubitus ulcer 9.4
1151 in situ carcinoma 9.4
1152 bacterial pneumonia 9.4
1153 rosacea 9.4
1154 autosomal dominant polycystic kidney disease 9.4
1155 hepatopulmonary syndrome 9.4
1156 leishmaniasis 9.4
1157 visceral leishmaniasis 9.4
1158 status asthmaticus 9.4
1159 keratoconjunctivitis 9.4
1160 encephalitis 9.4
1161 krukenberg carcinoma 9.4
1162 pathologic nystagmus 9.4
1163 placental abruption 9.4
1164 senile cataract 9.4
1165 biliary tract disease 9.4
1166 toxoplasmosis 9.4
1167 limb-girdle muscular dystrophy 9.4
1168 col1a1/2-related osteogenesis imperfecta 9.4
1169 charcot-marie-tooth neuropathy type 2a 9.4
1170 hypermobile ehlers-danlos syndrome 9.4
1171 noonan syndrome with multiple lentigines 9.4
1172 amaurosis fugax 9.4
1173 biliary tract cancer 9.4
1174 broken heart syndrome 9.4
1175 carcinoid syndrome 9.4
1176 charlie m syndrome 9.4
1177 chromosome 16q duplication 9.4
1178 chromosome 4p deletion 9.4
1179 congenital hydrocephalus 9.4
1180 congenitally corrected transposition of the great arteries 9.4
1181 coronary artery aneurysm 9.4
1182 depersonalization/derealization disorder 9.4
1183 dissociative seizures 9.4
1184 dock2 deficiency 9.4
1185 double discordia 9.4
1186 familial colorectal cancer 9.4
1187 gigantism 9.4
1188 hemorrhagic proctocolitis 9.4
1189 homologous wasting disease 9.4
1190 horseshoe kidney 9.4
1191 hypertrophic olivary degeneration 9.4
1192 kikuchi disease 9.4
1193 lichen sclerosus 9.4
1194 lymphosarcoma 9.4
1195 mediastinal endodermal sinus tumors 9.4
1196 neural crest tumor 9.4
1197 neurogenic hypertension 9.4
1198 papular mucinosis 9.4
1199 penis agenesis 9.4
1200 primary orthostatic tremor 9.4
1201 prostaglandin-endoperoxide synthase deficiency 9.4
1202 prosthetic joint infection 9.4
1203 reactive angioendotheliomatosis 9.4
1204 scleredema 9.4
1205 skeletal dysplasias 9.4
1206 spondyloenchondrodysplasia 9.4
1207 streptococcal group a invasive disease 9.4
1208 transposition of the great arteries 9.4
1209 trochlear dysplasia 9.4
1210 uniparental disomy of chromosome 2 9.4
1211 age-related hearing loss 9.4
1212 bunion 9.4
1213 multiple endocrine neoplasia 9.4
1214 opioid addiction 9.4
1215 pituitary tumors 9.4
1216 central cord syndrome 9.4
1217 cerebral hypoxia 9.4
1218 febrile seizures 9.4
1219 idiopathic central precocious puberty 9.4
1220 pouchitis 9.4
1221 paracetamol poisoning 9.4
1222 idiopathic avascular necrosis 9.4
1223 osteonecrosis of the jaw 9.4
1224 primitive portal vein thrombosis 9.4
1225 recurrent acute pancreatitis 9.4
1226 chronic pneumonitis of infancy 9.4
1227 microtia 9.4
1228 6-phosphogluconate dehydrogenase deficiency 9.4
1229 fibrocalculous pancreatopathy 9.4
1230 neurogenic thoracic outlet syndrome 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

Genetic Tests for Body Mass Index Quantitative Trait Locus 12

Genetic tests related to Body Mass Index Quantitative Trait Locus 12:

# Genetic test Affiliating Genes
1 Body Mass Index Quantitative Trait Locus 12 30 PCSK1

Anatomical Context for Body Mass Index Quantitative Trait Locus 12

MalaCards organs/tissues related to Body Mass Index Quantitative Trait Locus 12:

42
Bone, Heart, Liver, Breast, Pituitary, Prostate, Kidney

Publications for Body Mass Index Quantitative Trait Locus 12

Articles related to Body Mass Index Quantitative Trait Locus 12:

(showing 1, show less)
# Title Authors Year
1
Common nonsynonymous variants in PCSK1 confer risk of obesity. ( 18604207 )
2008

Variations for Body Mass Index Quantitative Trait Locus 12

ClinVar genetic disease variations for Body Mass Index Quantitative Trait Locus 12:

6 (showing 2, show less)
# Gene Variation Type Significance SNP ID Assembly Location
1 PCSK1 NM_000439.4(PCSK1): c.661A> G (p.Asn221Asp) single nucleotide variant Benign rs6232 GRCh37 Chromosome 5, 95751785: 95751785
2 PCSK1 NM_000439.4(PCSK1): c.661A> G (p.Asn221Asp) single nucleotide variant Benign rs6232 GRCh38 Chromosome 5, 96416081: 96416081

Expression for Body Mass Index Quantitative Trait Locus 12

Search GEO for disease gene expression data for Body Mass Index Quantitative Trait Locus 12.

Pathways for Body Mass Index Quantitative Trait Locus 12

GO Terms for Body Mass Index Quantitative Trait Locus 12

Sources for Body Mass Index Quantitative Trait Locus 12

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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