Raynaud disease

Preferred Label : Raynaud disease;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Cold fingers, hereditary;

Inheritance : Autosomal dominant;

Prefixed ID : %179600;

Details

Origin ID

179600;

UMLS CUI

C0034734;

Automatic exact mappings (from CISMeF team)
- Raynaud-like disorder [MedDRA LLT]
- atherosclerosis/peripheral vascular disease [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Primary Raynaud disease [ICD-11 Subcategory]
- Raynaud Phenomenon [NCIt concept]
- Raynaud disease [PASCAL descriptor]
- Raynaud disease [DO Concept]
- Raynaud disease [Disease (Nov.)]
- Raynaud phenomenon [HPO term]
- Raynaud's Disease [NCIt concept]
- Raynaud's disease [MedDRA LLT]
- Raynaud's disease (disorder) [SNOMED CT concept]
- Raynaud's syndrome [ICD-10 Sub-category]
- Raynauds syndrome [ICD-10 Sub-category (who)]
- raynaud disease [MeSH Descriptor]
- raynaud disease [MeSH concept]
- raynaud's disease [MedlinePlus Topic]
- raynaud's syndrome [SNOMED Notion]
DO Cross reference
- Raynaud disease [DO Concept]
HPO term(s)
- Abnormality of the skeletal system [HPO term]
- Autosomal dominant inheritance [HPO term]
- Raynaud phenomenon [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Primary Raynaud disease [ICD-11 Subcategory]
- Raynaud disease [DO Concept]
- Raynaud disease [PASCAL descriptor]
- Raynaud disease [Disease (Nov.)]
- Raynaud's Disease [NCIt concept]
- Raynaud's disease [MedDRA LLT]
- Raynaud's disease (disorder) [SNOMED CT concept]
- Raynauds [MedDRA LLT]
- Secondary Raynaud phenomenon [ICD-11 Subcategory]
- raynaud disease [MeSH Descriptor]
- raynaud disease [MeSH concept]
- raynaud's disease [MedlinePlus Topic]

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