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Diseases
Genes (1427)
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ABHD5
Cerebral Creatine Deficiency
RET
Pheochromocytoma
ABCD1
Adrenoleukodystrophy
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
SDHB
Pheochromocytoma
Uterine Fibroids
MAX
Pheochromocytoma
VHL
Pheochromocytoma
TMEM127
Pheochromocytoma
SDHD
Pheochromocytoma
KCNC3
Spinocerebellar Ataxia Type-13
GNAS
Pheochromocytoma
Mccune-Albright Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
TP53
Alopecia, Androgenetic, 1
Disseminated Superficial Actinic Porokeratosis
Pheochromocytoma
Uterine Fibroids
Epidermoid Cysts
GDNF
Pheochromocytoma
TP63
Placental Site Trophoblastic Tumor
Bladder Exstrophy
Uterine Fibroids
KIF1B
Pheochromocytoma
TSC2
Uterine Fibroids
STX3
Microvillus Inclusion Disease