loading...| Preferred Name |
systemic scleroderma |
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| Synonyms |
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| Definitions |
A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. |
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| ID |
http://purl.obolibrary.org/obo/DOID_418 |
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| definition |
A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. |
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| hasDbXref |
ICD9CM:710.1 SNOMEDCT_US_2016_03_01:89155008 SNOMEDCT_US_2016_03_01:156451000 SNOMEDCT_US_2016_03_01:201440007 SNOMEDCT_US_2016_03_01:128457007 UMLS_CUI:C0036421 MESH:D012595 EFO:0000717 NCI:C72070 ICD10CM:M34.0 ICD10CM:M34.9 SNOMEDCT_US_2016_03_01:268049000 |
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| hasExactSynonym |
Scleroderma progressive systemic sclerosis systemic sclerosis PSS (progressive systemic sclerosis) Scleroderma (& [systemic sclerosis]) Scleroderma syndrome |
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| hasOBONamespace |
disease_ontology |
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| id |
DOID:418 |
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| imported from | ||
| label |
systemic scleroderma |
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| prefixIRI |
DOID:418 |
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| prefLabel |
systemic scleroderma |
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| subClassOf |
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