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Diseases
Genes (1099)
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ABHD5
Cerebral Creatine Deficiency
UNC119
Immunodeficiency 13
Unc119 Lipid-Binding Chaperone
MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
TNFAIP3
Haploinsufficiency Of A20
FH
Hereditary Leiomyomatosis And Renal Cell Cancer
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
GAD1
Cerebral Palsy, Spastic Quadriplegic, 1
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
FGFR2
Squamous-Cell Carcinoma Of The Lung
STX3
Microvillus Inclusion Disease
EGFR
Squamous-Cell Carcinoma Of The Lung
DDR2
Squamous-Cell Carcinoma Of The Lung
AIPL1
Unc119 Lipid-Binding Chaperone
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
KRAS
Squamous-Cell Carcinoma Of The Lung