3-methylglutaconic aciduria type 3
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3-methylglutaconic aciduria type 3
Summary
3-methylglutaconic aciduria type 3 is a rare disease[1]. It draws 3 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2]
Key Facts
- 3-methylglutaconic aciduria type 3 is credited with the discovery of Hanan Costeff[3].
- 3-methylglutaconic aciduria type 3's instance of is recorded as rare disease[4].
- 3-methylglutaconic aciduria type 3's instance of is recorded as class of disease[5].
- Hanan Costeff is named after 3-methylglutaconic aciduria type 3[6].
- 3-methylglutaconic aciduria type 3's subclass of is recorded as 3-methylglutaconic aciduria[7].
- 3-methylglutaconic aciduria type 3's subclass of is recorded as syndromic hereditary optic neuropathy[8].
- 3-methylglutaconic aciduria type 3's subclass of is recorded as genetic disease[9].
- 3-methylglutaconic aciduria type 3's subclass of is recorded as autosomal recessive disease[10].
- 3-methylglutaconic aciduria type 3's subclass of is recorded as autosomal dominant optic atrophy and cataract[11].
- 3-methylglutaconic aciduria type 3's MeSH descriptor ID is recorded as C535311[12].
- 3-methylglutaconic aciduria type 3's OMIM ID is recorded as 258501[13].
- 3-methylglutaconic aciduria type 3's GeneReviews ID is recorded as NBK1473[14].
- 3-methylglutaconic aciduria type 3's Disease Ontology ID is recorded as DOID:0110004[15].
- 3-methylglutaconic aciduria type 3's Orphanet ID is recorded as 67047[16].
- 3-methylglutaconic aciduria type 3's genetic association is recorded as OPA3[17].
- 3-methylglutaconic aciduria type 3's Google Knowledge Graph ID is recorded as /g/122z2q4d[18].
- 3-methylglutaconic aciduria type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110004[19].
- 3-methylglutaconic aciduria type 3's exact match is recorded as http://identifiers.org/doid/DOID:0110004[20].
- 3-methylglutaconic aciduria type 3's UMLS CUI is recorded as C0574084[21].
- 3-methylglutaconic aciduria type 3's ICD-10-CM is recorded as E71.111[22].
- 3-methylglutaconic aciduria type 3's ICD-10-CM is recorded as E71.1[23].
- 3-methylglutaconic aciduria type 3's GARD rare disease ID is recorded as 5663[24].
- 3-methylglutaconic aciduria type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[25].
- 3-methylglutaconic aciduria type 3's Mondo ID is recorded as MONDO_0009787[26].
- 3-methylglutaconic aciduria type 3's Genetics Home Reference Conditions ID is recorded as costeff-syndrome[27].
Body
Works and Contributions
3-methylglutaconic aciduria type 3 is credited with the discovery of Hanan Costeff[3].
Why It Matters
3-methylglutaconic aciduria type 3 draws 3 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] It is known by 26 alternative names across languages and contexts.[29]