Histiocytosis, familial lipochrome

Preferred Label : Histiocytosis, familial lipochrome;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %235900;

Details

Origin ID

235900;

UMLS CUI

C0334125;

Currated CISMeF NLP mapping
- Lipochrome histiocytosis - familial (disorder) [SNOMED CT concept]
- histiocytosis, familial lipochrome [MeSH concept]
- histiocytosis, familial lipochrome [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Histiocytosis [HPO term]
- Increased alpha-globulin [HPO term]
- Increased circulating antibody level [HPO term]
- Polyarticular arthritis [HPO term]
- Pulmonary infiltrates [HPO term]
- Recurrent infections [HPO term]
- Susceptibility to infection [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lipochrome histiocytosis (morphologic abnormality) [SNOMED CT concept]
- Lipochrome histiocytosis - familial (disorder) [SNOMED CT concept]
- histiocytosis, familial lipochrome [MeSH Supplementary Concept]
- histiocytosis, familial lipochrome [MeSH concept]
- lipochrome histiocytosis [SNOMED Notion]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients