methylmalonic acidemia
Sign in to saveAlso known as METHYLMALONIC ACIDEMIA, cblA TYPE, METHYLMALONIC ACIDEMIA, cblB TYPE, METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY, METHYLMALONIC ACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN, cblA TYPE, METHYLMALONIC ACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN, cblB TYPE, METHYLMALONIC ACIDURIA, mut TYPE, METHYLMALONICACIDURIA DUE TO METHYLMALONIC CoA MUTASE deficiency, METHYLMALONICACIDURIA, vitamin B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN--cbl A
organic acidemia that involves an accumulation of methylmalonic acid in the blood
In the Vinony graph
Vinony's link graph records 129 inbound references to methylmalonic acidemia, and connects out to Online Mendelian Inheritance in Man, branched-chain amino acid and Methylmalonyl CoA epimerase.
Vinony files it under Amino acid metabolism disorders, Autosomal recessive disorders and Mitochondrial diseases.
Vinony links it to 12 Wikipedia language editions.
Wikidata facts
- Instance of
- inherited metabolic disorder
- Subclass of
- organic acidemia
Show 7 more facts
- external data available at URL
- www.nanbyou.or.jp/entry/4859
- health specialty
- endocrinology
- Commons category
- Methylmalonic acidemias
- exact match
- identifiers.org/doid/DOID:14749
- on focus list of Wikimedia project
- WikiProject Medicine
- NCI Thesaurus ID
- C98986
- ICD-9-CM
- 270.7
Sources (8)
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