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Diseases
Genes (213)
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ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
MMP21
Situs Ambiguus
ACVR2B
Situs Ambiguus
ZIC3
Situs Ambiguus
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
NODAL
Situs Ambiguus
CFAP53
Situs Ambiguus
LEFTY2
Situs Ambiguus
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
TNF
Manganism
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
KDM3B
Metal Toxicity
IL1B
Manganism
Renpenning's Syndrome
IFNG
Manganism
Vascular Tumor
BNIP3
Manganism