FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term CREST syndrome ID (Ontology) DOID:0060218 (Human Disease)
Definition A syndrome characterized by calcinosis, Raynaud's phenomeno, esophageal dysmotility, sclerodactyly and telangiectasia.
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
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship: 
  disease
   |__syndrome
       |__CREST syndrome
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
GARD:12430
ICD10CM:M34.1
MESH:D017675
NCI:C70646
SNOMEDCT_US_2023_03_01:31848007
SNOMEDCT_US_2023_03_01:62382002
UMLS_CUI:C0206138
UMLS_CUI:C1527226