CREST syndrome

disorder

SNOMED 31848007CUI C0206138

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormality of chromosome stability

HP:0003220

Abnormality of the abdomen

HP:0001438

Calcinosis

HP:0003761

Multiple chromosomal breaks

HP:0040012

Pseudoscleroderma

HP:0100324

Sclerodactyly

HP:0011838

Telangiectasia

HP:0001009

Related Conditions

Calcinosis cutis(parent)

Disorder of digit(parent)

Limited cutaneous systemic sclerosis(parent)

Disorder of soft tissue of limb(parent)

Systemic disease affecting skin(parent)

Cardiovascular disorder(parent)

Degenerative disorder of extremity(parent)

Quick Facts

SNOMED CT: 31848007
UMLS CUI: C0206138
Fully Specified Name: Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.