OBO ID: DOID:0060673
Term Name: Peters anomaly Search Ontology:
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)
OTHER Peters anomaly PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PAX6 Anterior segment dysgenesis 5, multiple subtypes 604229
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)