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Summary Literature (0)
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:

Referenced OMIM:
OMIM:0011414 - ANTERIOR SEGMENT DYSGENESIS 5; ASGD5
OMIM:604229 -

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : foxc1, foxe3, pitx2, pax6, cyp1b1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): corneal disease (is_a)


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