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Diseases
Genes (551)
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CAV3
Rippling Muscle Disease 1
Rippling Muscle Disease 2
TH
Tyrosine Hydroxylase Deficiency
Pheochromocytoma
TBC1D24
Doors Syndrome
Door Syndrome
LMX1B
Nail-Patella Syndrome
RET
Pheochromocytoma
MAX
Pheochromocytoma
VHL
Pheochromocytoma
TMEM127
Pheochromocytoma
SDHB
Pheochromocytoma
SDHD
Pheochromocytoma
ACO2
Infantile Cerebellar-Retinal Degeneration
SRPX2
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked
NALCN
Hypotonia-Speech Impairment-Severe Cognitive Delay Syndrome
PYCR2
Leukodystrophy, Hypomyelinating, 10
ATP6V1B2
Autosomal Dominant Deafness-Onychodystrophy Syndrome
GDNF
Pheochromocytoma
KIF1B
Pheochromocytoma
PLCB1
Early Infantile Epileptic Encephalopathy 12
TBX22
Congenital Radioulnar Synostosis
NF1
Fibrous Dysplasia Of Bone
Pheochromocytoma