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Diseases
Genes (610)
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ASL
Hyperoxia
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
IFIH1
Valvular Heart Disease
Singleton Merten Syndrome
Polymyositis
TNF
Hyperoxia
Valvular Heart Disease
Hypopigmentation
Polymyositis
IL1B
Erdheim–chester Disease
Hyperoxia
Valvular Heart Disease
Polymyositis
TIMP1
Hyperoxia
Valvular Heart Disease
Polymyositis
IL18
Hyperoxia
Valvular Heart Disease
Polymyositis
CYP1A1
Hyperoxia
HTR2B
Valvular Heart Disease
IL6
Hyperoxia
Argininosuccinic Aciduria
Polymyositis
BRAF
Erdheim–chester Disease
EPG5
Hypopigmentation
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CYP27B1
Tetany
Polymyositis
DDX58
Singleton Merten Syndrome
Polymyositis
TNFRSF1A
Hyperoxia
Polymyositis
SPP1
Erdheim–chester Disease
Valvular Heart Disease
FGFR1
Valvular Heart Disease
CCL2
Valvular Heart Disease
Polymyositis
AHR
Hyperoxia