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Diseases
Genes (1028)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
MYH7
Laing Distal Myopathy
PQBP1
Renpenning's Syndrome
SLC26A2
Atelosteogenesis, Type Ii
RHBDF2
Howel–evans Syndrome
TAP2
Bare Lymphocyte Syndrome, Type I
SHH
Holoprosencephaly
SIX3
Holoprosencephaly
TGIF1
Holoprosencephaly
GLI2
Holoprosencephaly
CD8A
Cd8 Deficiency, Familial
IFIH1
Singleton Merten Syndrome
NODAL
Holoprosencephaly
NRAS
Neurocutaneous Melanosis
TAPBP
Bare Lymphocyte Syndrome, Type I
TAP1
Bare Lymphocyte Syndrome, Type I
IDH2
Oligodendroglioma