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Diseases
Genes (1416)
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PMM2
Pmm2 Deficiency
Hyperinsulinism
ASL
Argininosuccinic Aciduria
ABCD1
Adrenoleukodystrophy
MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
KCNC3
Spinocerebellar Ataxia Type-13
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
LEP
Uterine Fibroids
Hyperinsulinism
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
TP63
Uterine Fibroids
Bladder Exstrophy
HMOX1
Adrenoleukodystrophy
Hyperinsulinism
TNF
Uterine Fibroids
Adrenoleukodystrophy
Lumbar Disc Disease
Hyperinsulinism
Familial Isolated Vitamin E Deficiency
TSC2
Uterine Fibroids
CCL2
Uterine Fibroids
Adrenoleukodystrophy
Hyperinsulinism
STX3
Microvillus Inclusion Disease
HMGA2
Uterine Fibroids
Hyperinsulinism
ESR1
Uterine Fibroids
Lumbar Disc Disease
Hyperinsulinism
INSR
Uterine Fibroids
Hyperinsulinism
MC4R
Hyperinsulinism