anterior segment dysgenesis 7
human disease
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anterior segment dysgenesis 7
Summary
anterior segment dysgenesis 7 is a rare disease[1].
Key Facts
- anterior segment dysgenesis 7's instance of is recorded as rare disease[2].
- anterior segment dysgenesis 7's instance of is recorded as class of disease[3].
- anterior segment dysgenesis 7's subclass of is recorded as autosomal recessive disease[4].
- anterior segment dysgenesis 7's subclass of is recorded as corneal opacification and other ocular anomalies[5].
- anterior segment dysgenesis 7's OMIM ID is recorded as 269400[6].
- anterior segment dysgenesis 7's Disease Ontology ID is recorded as DOID:0080612[7].
- anterior segment dysgenesis 7's Orphanet ID is recorded as 289499[8].
- anterior segment dysgenesis 7's genetic association is recorded as PXDN[9].
- anterior segment dysgenesis 7's Google Knowledge Graph ID is recorded as /g/11qqs1r3qp[10].
- anterior segment dysgenesis 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_289499[11].
- anterior segment dysgenesis 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080612[12].
- anterior segment dysgenesis 7's exact match is recorded as http://identifiers.org/doid/DOID:0080612[13].
- anterior segment dysgenesis 7's UMLS CUI is recorded as C1853235[14].
- anterior segment dysgenesis 7's UMLS CUI is recorded as C3151617[15].
- anterior segment dysgenesis 7's Mondo ID is recorded as MONDO_0010015[16].
- anterior segment dysgenesis 7's UniProt disease ID is recorded as DI-04168[17].