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Diseases
Genes (991)
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TTPA
Familial Isolated Vitamin E Deficiency
FAM20A
Enamel-Renal Syndrome
MYH7
Laing Distal Myopathy
PQBP1
Renpenning's Syndrome
SLC26A2
Atelosteogenesis, Type Ii
TP53
Adenoid Cystic Carcinoma
Bronchopulmonary Dysplasia
RHBDF2
Howel–evans Syndrome
SHH
Holoprosencephaly
SIX3
Holoprosencephaly
TGIF1
Holoprosencephaly
GLI2
Holoprosencephaly
IFIH1
Singleton Merten Syndrome
NODAL
Holoprosencephaly
NRAS
Neurocutaneous Melanosis
PTEN
Adenoid Cystic Carcinoma
Thrombophlebitis
Protein Losing Enteropathy
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
Holoprosencephaly
ZIC2
Holoprosencephaly
NOTCH1
Adenoid Cystic Carcinoma
PTCH1
Adenoid Cystic Carcinoma
Holoprosencephaly