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Diseases
Genes (545)
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ABHD5
Cerebral Creatine Deficiency
UNC119
Immunodeficiency 13
Unc119 Lipid-Binding Chaperone
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
TNFAIP3
Haploinsufficiency Of A20
FH
Hereditary Leiomyomatosis And Renal Cell Cancer
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
GAD1
Cerebral Palsy, Spastic Quadriplegic, 1
GALE
Galactose Epimerase Deficiency
MC2R
Familial Glucocorticoid Deficiency
CFH
Membranoproliferative Glomerulonephritis
STX3
Microvillus Inclusion Disease
TSLP
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
CTNS
Cystinosis
AIPL1
Unc119 Lipid-Binding Chaperone
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
MRAP
Familial Glucocorticoid Deficiency
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
SOST
Craniodiaphyseal Dysplasia