Results for "Hyperlipidemia, familial combined": 53 genes

Name

HYPLIP2 Gene

hyperlipidemia, combined, 2

AAA1 Gene

aortic aneurysm, familial abdominal 1

AAA3 Gene

Aneurysm, familial abdominal 3

AAA2 Gene

Aortic aneurysm, familial abdominal 2

AAA4 Gene

Aortic aneurysm, familial abdominal, 4

ETL6 Gene

Epilepsy, familial temporal lobe, 6

RCM2 Gene

cardiomyopathy, familial restrictive, 2

ATFB8 Gene

Atrial fibrillation, familial, 8

HNFJ3 Gene

Hyperuricemic nephropathy, familial juvenile, 3

GPSC Gene

gliosis, familial progressive subcortical

BHD Gene

Beukes familial hip dysplasia

FAME4 Gene

Epilepsy, familial adult myoclonic, 4

FAME3 Gene

Epilepsy, familial adult myoclonic, 3

PFHB2 Gene

Progressive familial heart block, type II

BFIS1 Gene

benign familial infantile convulsions

HBN1 Gene

Progressive familial heart block, type I, locus 1

ETL2 Gene

epilepsy, familial temporal lobe

FHII Gene

Hyperaldosteronism, familial, type II

FCMTE2 Gene

familial cortical myoclonic tremor with epilepsy 2

FCMTE1 Gene

familial cortical myoclonic tremor with epilepsy 1

GLM4 Gene

Glioma, familial, 1

PSHK2 Gene

Pseudohyperkalemia, familial, 2, due to red cell leak

VVS Gene

Syncope, familial vasovagal

BFIS4 Gene

Convulsions, benign familial infantile, 4

ATFB1 Gene

Atrial fibrillation, familial 1

ATFB2 Gene

familial atrial fibrillation 2

SXI2 Gene

X inactivation, familial skewed, 2

BFIC2 Gene

Benign familial infantile convulsions-2

FMTLE Gene

Epilepsy, familial mesial temporal lobe

STUT3 Gene

Stuttering, familial persistent, 3

STUT2 Gene

Stuttering, familial persistent 2

STUT1 Gene

Stuttering, familial persistent 1

STUT4 Gene

Stuttering, familial persistent, 4

BRCD1 Gene

cancer, familial, with in vitro radioresistance

MGR2 Gene

Migraine, familial typical, susceptibility to

MGR3 Gene

Migraine, familial, with or without aura, susceptibility to

MFT2 Gene

Trichoepithelioma, multiple familial, 2

FEB9 Gene

Febrile convulsions, familial, 9

ATFB5 Gene

Atrial fibrillation, familial, 5

HTGS Gene

Hypertriglyceridemia, familial

DIP Gene

interstitial pneumonitis, desquamative, familial

CMH21 Gene

Cardiomyopathy, familial hypertrophic, 21

CANDF1 Gene

candidiasis, familial 1

ATPLS Gene

antiphospholipid syndrome, familial

EOS Gene

eosinophilia, familial

FEB10 Gene

Febrile convulsions, familial, 10

LVNC2 Gene

noncompaction of left ventricular myocardium, familial isolated, autosomal dominant 2

THCYTX Gene

Thrombocytosis, familial X-linked

CMS1A1 Gene

myasthenia gravis, familial infantile, 1

BPPV Gene

vestibulopathy, familial

AAT2 Gene

Aortic aneurysm, familial thoracic 2

AAT1 Gene

Aortic aneurysm, familial thoracic 1

NKCD Gene

Natural killer cell deficiency, familial isolated