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Diseases
Genes (758)
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ABHD5
Cerebral Creatine Deficiency
ATP13A2
Kufor–rakeb Syndrome
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ADA2
Thrombocytosis
Sneddon Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
ITM2B
Retinal Dystrophy With Inner Retinal Dysfunction And Ganglion Cell Abnormalities
THPO
Thrombocytosis
MPL
Thrombocytosis
JAK2
Thrombocytosis
STX3
Microvillus Inclusion Disease
AR
Thrombocytosis
Pectus Excavatum
Alopecia, Androgenetic, 1
SRD5A2
Alopecia, Androgenetic, 1
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
CILP
Lumbar Disc Disease
TNFRSF10A
Alopecia, Androgenetic, 1
Lumbar Disc Disease
COL9A3
Lumbar Disc Disease