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anomaly (PA) is a congenital corneal opacity disorder characterized by a central corneal leukoma that obstructs the pupil leading to visual loss as well as absence of the posterior corneal stroma and Descemet membrane. [Orphanet:708]","descendants":["MONDO:0020353","MONDO:0015095"],"excluded_subClassOf":{"mondo":["MONDO:0020220"]},"has_material_basis_in_germline_mutation_in":{"http":["http://identifiers.org/hgnc/8620"]},"label":"Peters anomaly","mondo":"MONDO:0011414","parents":["MONDO:0000942","MONDO:0019503"],"synonym":{"exact":["anterior segment dysgenesis 5, multiple subtypes","Peters anomaly","Peters anomaly (disease)","Peters congenital glaucoma"],"related":["ASGD5"]},"xrefs":{"doid":["DOID:0060673","DOID:0080610"],"gard":["0007377"],"hp":["HP:0000659"],"icd11":["foundation:1902926622"],"icd9":["743.44"],"meddra":["10059202"],"medgen":["91031"],"mesh":["C537884"],"omim":["604229"],"orphanet":["708"],"sctid":["204153003"],"umls":["C0344559"]}},"original_id":"orphanet:708","umls":{"_license":"https://www.nlm.nih.gov/research/umls/knowledge_sources/metathesaurus/release/license_agreement.html","icd10cm":{"non-preferred":"Q13.4"},"mesh":{"non-preferred":"C537884"},"snomed":{"non-preferred":["204153003","86628002"],"preferred":"204153003"},"umls":"C0344559"}}