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Disease association ontology term - MONDO:0016826 - methylmalonic aciduria and homocystinuria

Term summary

ID
MONDO:0016826
Name
methylmalonic aciduria and homocystinuria
Ontology or CV name
Disease association
Definition
An inborn error of vitamin B12 (cobalamin) metabolism characterized by megaloblastic anemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures. There are four complementation classes of cobalamin defects (cblC, cblD, cblF and cblJ) that are responsible for methylmalonic acidemia - homocystinuria (methylmalonic acidemia - homocystinuria cblC, cblD cblF and cblJ).

Parents

Annotation

Disease association

MONDO:0010184 - methylmalonic aciduria and homocystinuria type cblC

References:

Genes: