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DOID:0060673 - Peters anomaly
Disease Ontology 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.
Synonyms:
Xenbase Genes
:
foxc1,
foxe3,
pitx2,
pax6,
cyp1b1
| MONDO:0011414 - Peters anomaly |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
corneal disease (is_a)