Limited cutaneous systemic sclerosis

disorder

SNOMED 298285004CUI C5574860

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.

Abnormal skin colour

Very frequent (80-99%)HP:0001000

Autoimmune disorder

Very frequent (80-99%)HP:0002960

Dermatopathy

Very frequent (80-99%)HP:0000951

Hypopigmented skin patches

Very frequent (80-99%)HP:0001053

Narrow foramen obturatorium

Very frequent (80-99%)HP:0100958

Deglutition disorder

Frequent (30-79%)HP:0002015

Gastro-esophageal reflux

Frequent (30-79%)HP:0002020

Mucosal telangiectasiae

Frequent (30-79%)HP:0100579

Nausea and vomiting

Frequent (30-79%)HP:0002017

Open skin sore

Frequent (30-79%)HP:0200042

Teleangiectasia of the skin

Frequent (30-79%)HP:0100585

Contractures of the hands

Occasional (5-29%)HP:0009473

Foot joint contracture

Occasional (5-29%)HP:0008366

Pulmonary artery hypertension

Occasional (5-29%)HP:0002092

Pulmonary fibrosis

Occasional (5-29%)HP:0002206

Related Conditions

CREST syndrome(child)

CRST syndrome(child)

Primary biliary cirrhosis co-occurrent with systemic scleroderma(child)

Limited systemic sclerosis(parent)

Quick Facts

SNOMED CT: 298285004
UMLS CUI: C5574860
Fully Specified Name: Systemic sclerosis with limited cutaneous involvement (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.