molybdenum cofactor deficiency, complementation group C

Preferred Label : molybdenum cofactor deficiency, complementation group C;

MeSH synonym : Molybdenum Cofactor Deficiency Type C;

Origin ID

C565374;

UMLS CUI

C1854990;

Currated CISMeF NLP mapping
- Molybdenum Cofactor deficiency, type C [OMIM Phenotype]
- Molybdenum cofactor deficiency complementation group C (disorder) [SNOMED CT concept]
- Molybdenum cofactor deficiency, complementation group C [ICD-11 More detail]
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C [ORDO Disease]
- molybdenum cofactor deficiency type C [DO Concept]
DO Cross reference
- molybdenum cofactor deficiency type C [DO Concept]
MeSH term(s) associated for indexing
- metal metabolism, inborn errors [MeSH Descriptor]
- molybdoferredoxin [MeSH Descriptor]
Record concept(s)
- molybdenum cofactor deficiency, complementation group C [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Molybdenum Cofactor deficiency, type C [OMIM Phenotype]
- Molybdenum cofactor deficiency complementation group C (disorder) [SNOMED CT concept]
- Molybdenum cofactor deficiency, complementation group C [ICD-11 More detail]
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C [ORDO Disease]
- molybdenum cofactor deficiency type C [DO Concept]