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Diseases
Genes (1082)
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PAX6
Aniridia 2
TTPA
Familial Isolated Vitamin E Deficiency
FAM20A
Enamel-Renal Syndrome
MYH7
Laing Distal Myopathy
TP53
Poorly Differentiated Thyroid Cancer
Adenoid Cystic Carcinoma
Bronchopulmonary Dysplasia
PQBP1
Renpenning's Syndrome
SLC26A2
Atelosteogenesis, Type Ii
TRIM44
Aniridia 2
RHBDF2
Howel–evans Syndrome
SHH
Holoprosencephaly
SIX3
Holoprosencephaly
TGIF1
Holoprosencephaly
GLI2
Holoprosencephaly
IFIH1
Singleton Merten Syndrome
NRAS
Aniridia 2
Poorly Differentiated Thyroid Cancer
Neurocutaneous Melanosis
NODAL
Holoprosencephaly
WT1
Aniridia 2
PTEN
Adenoid Cystic Carcinoma
Thrombophlebitis
Protein Losing Enteropathy
FOXC1
Aniridia 2
ELP4
Aniridia 2