Benign familial copper deficiency

Preferred Label : Benign familial copper deficiency;

ICD-11 definition : This is a benign familial very rare hematological and neurological disorder. The disease involves a nutritional deficiency in the trace element copper. Copper is ubiquitous and daily requirement is low making acquired copper deficiency very rare. Copper deficiency can manifest in parallel with vitamin B12 and other nutritional deficiencies .;

Détails

Origin ID

580108812;

UMLS CUI

C1852576;

Currated CISMeF NLP mapping
- Copper deficiency, familial benign [MeSH concept]
- Copper deficiency, familial benign [OMIM Phenotype]
- Familial benign copper deficiency [ORDO Disease]
- Familial benign copper deficiency (disorder) [SNOMED CT concept]
- copper deficiency, familial benign [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Copper deficiency, familial benign [OMIM Phenotype]
- Copper deficiency, familial benign [MeSH concept]
- Familial benign copper deficiency [ORDO Disease]
- Familial benign copper deficiency (disorder) [SNOMED CT concept]
- copper deficiency, familial benign [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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