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Human Disease

Peters anomaly

Term ID
DOID:0060673
Synonyms
Definition
A corneal disease characterized by a central corneal leukoma and absence of the posterior corneal stroma and Descemet membrane that has_material_basis_in mutation in the PAX6 gene on chromosome 11p13, the PITX2 gene on chromosome 4q25, the CYP1B1 gene on chromosome 2p22.2, or the FOXC1 gene on chromosome 6p25.3. (3)
References
Ontology
Human Disease   ( DOID:0060673 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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