Search Ontology:
Human Disease

mild variant of maple syrup urine disease

Term ID
DOID:0061205
Synonyms
Definition
A maple syrup urine disease characterized by increased plasma levels of branched-chain amino acids (BCAA) apparent at birth that has_material_basis_in homozygous mutation in the PPM1K gene on chromosome 4q22. https://pubmed.ncbi.nlm.nih.gov/23086801/
References
Ontology
Human Disease   ( DOID:0061205 )
Relationships
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Genes Involved
Zebrafish Models