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Human Disease
methylmalonic aciduria and homocystinuria type cblG
- Term ID
- DOID:0050733
- Synonyms
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- Definition
- A methylmalonic acidemia that is characterized by megaloblastic anemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures, has_material_basis_in homozygous or compound heterozygous mutation in the MTR gene on chromosome 1q43 that causes an inborn error of vitamin B12 metabolism. (2)
- References
- Ontology
- Human Disease ( DOID:0050733 )
- is a type of
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Genes Involved
Zebrafish Models