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Diseases
Genes (1011)
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TTPA
Familial Isolated Vitamin E Deficiency
Hyperoxia
ABCD1
Adrenoleukodystrophy
KCNC3
Spinocerebellar Ataxia Type-13
TNF
Adrenoleukodystrophy
Hyperinsulinism
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Hyperoxia
Morphea
PQBP1
Renpenning's Syndrome
LEP
Hyperinsulinism
IFIH1
Singleton Merten Syndrome
TP63
Bladder Exstrophy
HMOX1
Adrenoleukodystrophy
Hyperinsulinism
CCL2
Adrenoleukodystrophy
Hyperinsulinism
NOS3
Hyperinsulinism
Familial Isolated Vitamin E Deficiency
Hyperoxia
CD55
Protein Losing Enteropathy
SOD2
Adrenoleukodystrophy
Hyperoxia
INSR
Hyperinsulinism
CYP1A1
Hyperoxia
MC4R
Hyperinsulinism
ISL1
Bladder Exstrophy
LMNA
Hyperinsulinism
Morphea
LEPR
Hyperinsulinism
RB1
Pinealoblastoma
Trilateral Retinoblastoma