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Diseases
Genes (664)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
IFIH1
Valvular Heart Disease
Singleton Merten Syndrome
Polymyositis
MC2R
Familial Glucocorticoid Deficiency
TNF
Alopecia, Androgenetic, 1
Valvular Heart Disease
Hypopigmentation
Lumbar Disc Disease
Polymyositis
IL1B
Alopecia, Androgenetic, 1
Valvular Heart Disease
Epidermoid Cysts
Polymyositis
RHOA
Alopecia, Androgenetic, 1
Hypopigmentation
STX3
Microvillus Inclusion Disease
HTR2B
Valvular Heart Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
CYP27B1
Alopecia, Androgenetic, 1
Tetany
Polymyositis
EPG5
Hypopigmentation
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
Epidermoid Cysts
CILP
Lumbar Disc Disease
DDX58
Singleton Merten Syndrome
Polymyositis