autosomal dominant optic atrophy plus syndrome
human disease
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autosomal dominant optic atrophy plus syndrome
Summary
autosomal dominant optic atrophy plus syndrome is a class of disease[1].
Key Facts
- autosomal dominant optic atrophy plus syndrome's instance of is recorded as class of disease[2].
- autosomal dominant optic atrophy plus syndrome's subclass of is recorded as autosomal dominant optic atrophy[3].
- autosomal dominant optic atrophy plus syndrome's subclass of is recorded as syndrome[4].
- autosomal dominant optic atrophy plus syndrome's subclass of is recorded as autosomal dominant disease[5].
- autosomal dominant optic atrophy plus syndrome's MeSH descriptor ID is recorded as C535351[6].
- autosomal dominant optic atrophy plus syndrome's Disease Ontology ID is recorded as DOID:0111340[7].
- autosomal dominant optic atrophy plus syndrome's Orphanet ID is recorded as 1215[8].
- autosomal dominant optic atrophy plus syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1215[9].
- autosomal dominant optic atrophy plus syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111340[10].
- autosomal dominant optic atrophy plus syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111340[11].
- autosomal dominant optic atrophy plus syndrome's UMLS CUI is recorded as C1832466[12].
- autosomal dominant optic atrophy plus syndrome's ICD-10-CM is recorded as H47.2[13].
- autosomal dominant optic atrophy plus syndrome's Mondo ID is recorded as MONDO_0014720[14].
- autosomal dominant optic atrophy plus syndrome's ICD-11 ID is recorded as 1149710475[15].
- autosomal dominant optic atrophy plus syndrome's UniProt disease ID is recorded as DI-02096[16].