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Diseases
Genes (462)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
SLC12A6
Andermann Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
CRH
Alopecia, Androgenetic, 1
Melancholia
MTHFR
Alopecia, Androgenetic, 1
Melancholia
PON1
Melancholia
Membranoproliferative Glomerulonephritis
ALB
Melancholia
Membranoproliferative Glomerulonephritis
CFH
Membranoproliferative Glomerulonephritis
Salmonellosis
SLC6A4
Melancholia
STX3
Microvillus Inclusion Disease
TSLP
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
POMC
Melancholia
Familial Glucocorticoid Deficiency