3-methylglutaconic aciduria type 3
3-methylglutaconic aciduria that has material basis in mutation in the OPA3 gene
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3-methylglutaconic aciduria type 3
Summary
3-methylglutaconic aciduria type 3 is a rare disease[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[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 is a type of 3-methylglutaconic aciduria[7].
- 3-methylglutaconic aciduria type 3 is a type of syndromic hereditary optic neuropathy[8].
- 3-methylglutaconic aciduria type 3 is a type of genetic disease[9].
- 3-methylglutaconic aciduria type 3 is a type of autosomal recessive disease[10].
- 3-methylglutaconic aciduria type 3 is a type of autosomal dominant optic atrophy and cataract[11].
- 3-methylglutaconic aciduria type 3's genetic association is recorded as OPA3[12].
- 3-methylglutaconic aciduria type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110004[13].
- 3-methylglutaconic aciduria type 3's exact match is recorded as http://identifiers.org/doid/DOID:0110004[14].
- 3-methylglutaconic aciduria type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
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 has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 26 alternative names across languages and contexts.[16]