Molybdenum cofactor deficiency, complementation group B

Preferred Label : Molybdenum cofactor deficiency, complementation group B;

ICD-11 synonym : Molybdenum cofactor deficiency due tio defects in MOCS2 gene;

Details

Origin ID

344434559;

UMLS CUI

C1854989;

Currated CISMeF NLP mapping
- Molybdenum cofactor deficiency complementation group B (disorder) [SNOMED CT concept]
- Molybdenum cofactor deficiency, type b [OMIM Phenotype]
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B [ORDO Disease]
- molybdenum cofactor deficiency type B [DO Concept]
- molybdenum cofactor deficiency, complementation group B [MeSH concept]
- molybdenum cofactor deficiency, complementation group B [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Molybdenum cofactor deficiency complementation group B (disorder) [SNOMED CT concept]
- Molybdenum cofactor deficiency, type b [OMIM Phenotype]
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B [ORDO Disease]
- molybdenum cofactor deficiency type B [DO Concept]
- molybdenum cofactor deficiency, complementation group B [MeSH concept]
- molybdenum cofactor deficiency, complementation group B [MeSH Supplementary Concept]

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