molybdenum cofactor deficiency, complementation group A

Preferred Label : molybdenum cofactor deficiency, complementation group A;

MeSH synonym : Molybdenum Cofactor Deficiency Type A;

Origin ID

C565372;

UMLS CUI

C1854988;

Currated CISMeF NLP mapping
- Molybdenum cofactor deficiency complementation group A (disorder) [SNOMED CT concept]
- Molybdenum cofactor deficiency, complementation group A [ICD-11 More detail]
- Molybdenum cofactor deficiency, type a [OMIM Phenotype]
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency [ICD-11 More detail]
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A [ORDO Disease]
- molybdenum cofactor deficiency type A [DO Concept]
DO Cross reference
- molybdenum cofactor deficiency type A [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 A [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Molybdenum cofactor deficiency complementation group A (disorder) [SNOMED CT concept]
- Molybdenum cofactor deficiency, complementation group A [ICD-11 More detail]
- Molybdenum cofactor deficiency, type a [OMIM Phenotype]
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A [ORDO Disease]
- molybdenum cofactor deficiency type A [DO Concept]
Validated automatic mappings to NTBT
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency [ORDO Disease]