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Diseases
Genes (1772)
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ABCD1
Adrenoleukodystrophy
PMM2
Pmm2 Deficiency
Hyperinsulinism
RET
Pheochromocytoma
Primary Aldosteronism
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
TNF
Adrenoleukodystrophy
Pheochromocytoma
Myotonic Dystrophy
Hyperinsulinism
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Morphea
Uterine Fibroids
MED12
Fg Syndrome
Uterine Fibroids
SDHB
Pheochromocytoma
Uterine Fibroids
MAX
Pheochromocytoma
VHL
Pheochromocytoma
TMEM127
Pheochromocytoma
SDHD
Pheochromocytoma
KCNC3
Spinocerebellar Ataxia Type-13
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
LEP
Pheochromocytoma
Hyperinsulinism
Uterine Fibroids
IFIH1
Singleton Merten Syndrome
GDNF
Pheochromocytoma
TP53
Pheochromocytoma
Myotonic Dystrophy
Hyperinsulinism
Morphea
Uterine Fibroids