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Diseases
Genes (519)
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ABHD5
Cerebral Creatine Deficiency
TP53
Alopecia, Androgenetic, 1
Disseminated Superficial Actinic Porokeratosis
Li–fraumeni Syndrome
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ABCC9
Cantú Syndrome
MC2R
Familial Glucocorticoid Deficiency
Hyperkalemia
MED12
Fg Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
RECQL4
Li–fraumeni Syndrome
Baller–gerold Syndrome
CHEK2
Li–fraumeni Syndrome
KCNJ8
Cantú Syndrome
CFH
Membranoproliferative Glomerulonephritis
STX3
Microvillus Inclusion Disease
TSLP
Lumbar Disc Disease
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
MRAP
Familial Glucocorticoid Deficiency
Hyperkalemia
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
Li–fraumeni Syndrome
RB1
Pinealoblastoma
Li–fraumeni Syndrome
Trilateral Retinoblastoma
MDM2
Cerebral Creatine Deficiency
Li–fraumeni Syndrome