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Diseases
Genes (680)
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RET
Pheochromocytoma
DBH
Pheochromocytoma
Dopamine Beta Hydroxylase Deficiency
NGF
Pheochromocytoma
Neuropathy, Hereditary Sensory, Type Id
Neuropathy, Hereditary Sensory And Autonomic, Type V
Indifference To Pain, Congenital, Autosomal Recessive
ASL
Argininosuccinic Aciduria
PRDM12
Neuropathy, Hereditary Sensory And Autonomic, Type V
Hereditary Sensory And Autonomic Neuropathy Type 8
NTRK1
Pheochromocytoma
Neuropathy, Hereditary Sensory, Type Id
Neuropathy, Hereditary Sensory And Autonomic, Type V
Indifference To Pain, Congenital, Autosomal Recessive
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
LRSAM1
Charcot-Marie-Tooth Disease Type 2p
MAX
Pheochromocytoma
VHL
Pheochromocytoma
TMEM127
Pheochromocytoma
SDHB
Pheochromocytoma
SDHD
Pheochromocytoma
SCN9A
Neuropathy, Hereditary Sensory And Autonomic, Type V
Indifference To Pain, Congenital, Autosomal Recessive
SPTLC1
Neuropathy, Hereditary Sensory, Type Id
PQBP1
Renpenning's Syndrome
GDNF
Pheochromocytoma
HR
Alopecia Areata 1