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Diseases
Genes (948)
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SHH
Cyclopia
Holoprosencephaly
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
SIX3
Cyclopia
Holoprosencephaly
MYH7
Laing Distal Myopathy
TGIF1
Cyclopia
Holoprosencephaly
GLI2
Cyclopia
Holoprosencephaly
PQBP1
Renpenning's Syndrome
SLC26A2
Atelosteogenesis, Type Ii
RHBDF2
Howel–evans Syndrome
NODAL
Cyclopia
Holoprosencephaly
TAP2
Bare Lymphocyte Syndrome, Type I
CD8A
Cd8 Deficiency, Familial
IFIH1
Singleton Merten Syndrome
ZIC2
Cyclopia
Holoprosencephaly
NRAS
Neurocutaneous Melanosis
TAPBP
Bare Lymphocyte Syndrome, Type I
TAP1
Bare Lymphocyte Syndrome, Type I