biotin deficiency

Preferred Label : biotin deficiency;

CISMeF synonym : late-onset multiple carboxylase deficiency;

Origin ID

C531633;

UMLS CUI

C0268680;

Automatic exact mappings (from CISMeF team)
- Biotin deficiency [ICD-11 Category]
- Deficiency of other specified B group vitamins [ICD-10 Sub-category (who)]
- Deficiency of other specified B group vitamins [ICD-10 Sub-category]
Currated CISMeF NLP mapping
- Biotin deficiency [PASCAL descriptor]
- Biotin deficiency [MedDRA Preferred Term]
- Biotin deficiency (disorder) [SNOMED CT concept]
- Biotin deficiency disease (disorder) [SNOMED CT concept]
- Biotinidase Deficiency [NCIt concept]
- Biotinidase deficiency [OMIM Phenotype]
- Biotinidase deficiency [LOINC component]
- Biotinidase deficiency [ORDO Disease]
- Biotinidase deficiency (disorder) [SNOMED CT concept]
- Deficiency of biotin (disorder) [SNOMED CT concept]
- biotin deficiency [DO Concept]
- biotinidase deficiency [DO Concept]
DO Cross reference
- biotin deficiency [DO Concept]
MeSH term(s) associated for indexing
- biotinidase deficiency [MeSH Descriptor]
Record concept(s)
- Biotin deficiency [MeSH concept]
See also inter- (CISMeF)
- Multiple carboxylase deficiency due to biotinidase deficiency [ICD-11 More detail]
- biotinidase deficiency [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Biotin deficiency [MedDRA Preferred Term]
- Biotin deficiency (disorder) [SNOMED CT concept]
- Deficiency of biotin (disorder) [SNOMED CT concept]