multiple carboxylase deficiency
MONDO:0015454Mondo
Findings
No curated finding names multiple carboxylase deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Multiple carboxylase deficiency (MCD) is a term used to describe inborn errors of biotin metabolism characterized by reduced activities of biotin-dependent enzymes resulting in a wide spectrum of symptoms, including feeding difficulty, breathing difficulties, lethargy, seizures, skin rash, alopecia, and developmental delay.
Definition from the Mondo Disease Ontology (MONDO:0015454), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
1 name
Resolves to: multiple carboxylase deficiency
- Also called
- MCD