FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term systemic scleroderma ID (Ontology) DOID:418 (Human Disease)
Definition A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." [url:https\://ghr.nlm.nih.gov/condition/systemic-scleroderma] {comment="sn:IEDB"}
Also Known As "progressive systemic sclerosis" ; "Scleroderma" ; "Scleroderma syndrome" (for all, see Synonyms field below)
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 for disease ribbon | pseudopseudohypoparathyroidism       2
 model of | pseudopseudohypoparathyroidism       2
Spanning Tree (Parents/Children)
Only view relationship: 
  rheumatic disease
   |__scleroderma
       |__systemic scleroderma
           |__diffuse scleroderma
           |__limited scleroderma
           |__pulmonary systemic sclerosis
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a scleroderma
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "progressive systemic sclerosis" EXACT
    "Scleroderma" EXACT
    "Scleroderma syndrome" EXACT
    "systemic sclerosis" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
EFO:0000717
GARD:9748
ICD10CM:M34.0
ICD9CM:710.1
MESH:D012595
MIM:181750
NCI:C72070
SNOMEDCT_US_2023_03_01:89155008
UMLS_CUI:C0036421