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Diseases
Genes (662)
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SHH
Cyclopia
Holoprosencephaly
TTPA
Familial Isolated Vitamin E Deficiency
MMUT
Methylmalonyl-Coa Mutase Deficiency
SIX3
Cyclopia
Holoprosencephaly
TGIF1
Cyclopia
Holoprosencephaly
GLI2
Cyclopia
Holoprosencephaly
PQBP1
Renpenning's Syndrome
SLC2A1
Glut1 Deficiency
GNAQ
Sturge–weber Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
NODAL
Cyclopia
Holoprosencephaly
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
ZIC2
Cyclopia
Holoprosencephaly
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CDON
Cyclopia
Holoprosencephaly
PTCH1
Cyclopia
Holoprosencephaly
RASA1
Sturge–weber Syndrome