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Diseases
Genes (1605)
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RET
Pheochromocytoma
Pectus Excavatum
ATP13A2
Kufor–rakeb Syndrome
ABCD1
Adrenoleukodystrophy
TTPA
Familial Isolated Vitamin E Deficiency
SDHB
Pheochromocytoma
Pectus Excavatum
SDHD
Pheochromocytoma
Pectus Excavatum
DMD
Pectus Excavatum
Muscular Dystrophy, Becker Type
PQBP1
Pectus Excavatum
Renpenning's Syndrome
MAX
Pheochromocytoma
VHL
Pheochromocytoma
TMEM127
Pheochromocytoma
CCL2
Adrenoleukodystrophy
Muscular Dystrophy, Becker Type
Hyperinsulinism
ADA2
Thrombocytosis
Sneddon Syndrome
KCNC3
Spinocerebellar Ataxia Type-13
LEP
Pheochromocytoma
Hyperinsulinism
GDNF
Pheochromocytoma
ITM2B
Retinal Dystrophy With Inner Retinal Dysfunction And Ganglion Cell Abnormalities
IFIH1
Singleton Merten Syndrome
KIF1B
Pheochromocytoma
TP63
Pectus Excavatum
Bladder Exstrophy