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Diseases
Genes (497)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
IFIH1
Valvular Heart Disease
Singleton Merten Syndrome
Polymyositis
TNF
Valvular Heart Disease
Hypopigmentation
Polymyositis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
IL1B
Erdheim–chester Disease
Valvular Heart Disease
Polymyositis
Renpenning's Syndrome
HTR2B
Valvular Heart Disease
BRAF
Erdheim–chester Disease
EPG5
Hypopigmentation
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CYP27B1
Tetany
Polymyositis
CST3
Cerebral Amyloid Angiopathy
SPP1
Erdheim–chester Disease
Valvular Heart Disease
Cerebral Amyloid Angiopathy
DDX58
Singleton Merten Syndrome
Polymyositis
KDM3B
Metal Toxicity
FGFR1
Valvular Heart Disease
CCL2
Valvular Heart Disease
Polymyositis
TIMP1
Valvular Heart Disease
Polymyositis
IL18
Valvular Heart Disease
Polymyositis