ornithine translocase deficiency
amino acid metabolic disorder that has material basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood
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ornithine translocase deficiency
Summary
ornithine translocase deficiency is a rare disease[1]. It draws 15 Wikipedia views per month (rare_disease category, ranking #223 of 627).[2]
Key Facts
- ornithine translocase deficiency's instance of is recorded as rare disease[3].
- ornithine translocase deficiency's instance of is recorded as class of disease[4].
- ornithine translocase deficiency's subclass of is recorded as amino acid metabolic disorder[5].
- ornithine translocase deficiency's subclass of is recorded as infectious disease[6].
- ornithine translocase deficiency's MeSH descriptor ID is recorded as C538380[7].
- ornithine translocase deficiency's OMIM ID is recorded as 238970[8].
- ornithine translocase deficiency's ICD-9 ID is recorded as 270.6[9].
- ornithine translocase deficiency's DiseasesDB is recorded as 29849[10].
- ornithine translocase deficiency's KEGG ID is recorded as H01268[11].
- ornithine translocase deficiency's Disease Ontology ID is recorded as DOID:0050720[12].
- ornithine translocase deficiency's Orphanet ID is recorded as 415[13].
- ornithine translocase deficiency's NCI Thesaurus ID is recorded as C129029[14].
- ornithine translocase deficiency's different from is recorded as Hhhh syndrome[15].
- ornithine translocase deficiency's genetic association is recorded as SLC25A15[16].
- ornithine translocase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050720[17].
- ornithine translocase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0050720[18].
- ornithine translocase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_415[19].
- ornithine translocase deficiency's UMLS CUI is recorded as C0268540[20].
- ornithine translocase deficiency's ICD-10-CM is recorded as E72.4[21].
- ornithine translocase deficiency's GARD rare disease ID is recorded as 2830[22].
- ornithine translocase deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].
- ornithine translocase deficiency's Mondo ID is recorded as MONDO_0009393[24].
- ornithine translocase deficiency's Microsoft Academic ID is recorded as 2778727777[25].
- ornithine translocase deficiency's Genetics Home Reference Conditions ID is recorded as ornithine-translocase-deficiency[26].
- ornithine translocase deficiency's ICD-11 ID is recorded as 1193271821[27].
Why It Matters
ornithine translocase deficiency draws 15 Wikipedia views per month (rare_disease category, ranking #223 of 627).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] It is known by 9 alternative names across languages and contexts.[29]