familial disease, nos

Preferred Label : familial disease, nos;

Origin ID

DF-00190;

UMLS CUI

C0277558;

Automatic exact mappings (from CISMeF team)
- Familial disease [PASCAL descriptor]
- Family illness (situation) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Familial disease (disorder) [SNOMED CT concept]
Décrit
- cherubism [SNOMED Notion]
- familial acantholysis [SNOMED Notion]
- familial cardiomyopathy [SNOMED Notion]
- familial duodenal ulcer associated with rapid gastric emptying [SNOMED Notion]
- familial hypergastrinemic duodenal ulcer [SNOMED Notion]
- familial multiple polyposis syndrome [SNOMED Notion]
- familial osteoarthropathy of the fingers [SNOMED Notion]
- familial pericarditis [SNOMED Notion]
- normopepsinogenemic familial duodenal ulcer [SNOMED Notion]
- primary familial dilated cardiomyopathy [SNOMED Notion]
- primary familial hypertrophic cardiomyopathy [SNOMED Notion]
- white sponge nevus of mucosa [SNOMED Notion]
ICD-10 exact mapping(s)
- Unknown and unspecified causes of morbidity [ICD-10 category (who)]
Metaterm(s)
- genetics [CISMeF Metaterm]
SNOMED CT concept
- Familial disease (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial disease (disorder) [SNOMED CT concept]
- familial disorder [Disease (Nov.)]