C142171Level 7
Methylmalonic Aciduria, cblA Type
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal recessive form of methylmalonic aciduria, caused by mutation(s) in the MMAA gene, encoding MMAA protein.
GET
/api/v1/systems/nci_thesaurus/nodes/C142171Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.