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loading...| Preferred Name |
Raynaud disease |
| Synonyms |
Raynaud's syndrome |
| Definitions |
A peripheral vascular disease that is characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or cyanosis in response to cold exposure or stress. OMIM mapping confirmed by DO. [SN]. |
| ID |
http://purl.obolibrary.org/obo/DOID_10300 |
| comment |
OMIM mapping confirmed by DO. [SN]. |
| database_cross_reference |
OMIM:179600 MESH:D011928 UMLS_CUI:C0034734 ICD10CM:I73.0 SNOMEDCT_US_2022_09_01:195295006 |
| definition |
A peripheral vascular disease that is characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or cyanosis in response to cold exposure or stress. |
| has exact match |
MESH:D011928 |
| has exact synonym |
Raynaud's syndrome Raynaud's disease |
| has_obo_namespace |
disease_ontology |
| id |
DOID:10300 |
| label |
Raynaud disease |
| notation |
DOID:10300 |
| prefLabel |
Raynaud disease |
| subClassOf |
Create New Mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MESH/D011928 | Medical Subject Headings | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/179600 | Online Mendelian Inheritance in Man | LOOM |