Jump to:
loading...| Preferred Name |
systemic scleroderma |
|
| Synonyms |
Scleroderma systemic sclerosis |
|
| Definitions |
A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_418 |
|
| database_cross_reference |
SNOMEDCT_US_2023_03_01:89155008 MESH:D012595 UMLS_CUI:C0036421 ICD10CM:M34.0 EFO:0000717 ICD9CM:710.1 GARD:9748 MIM:181750 NCI:C72070 |
|
| definition |
A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. |
|
| has exact synonym |
Scleroderma progressive systemic sclerosis Scleroderma syndrome systemic sclerosis |
|
| has symptom | ||
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:418 |
|
| in_subset | ||
| label |
systemic scleroderma |
|
| notation |
DOID:418 |
|
| prefLabel |
systemic scleroderma |
|
| subClassOf |
Create mapping