Gastrocutaneous syndrome

disorder

SNOMED 782946000CUI C1850899

Overview

Gastrocutaneous syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Increased distance between eyes

Very frequent (80-99%)HP:0000316

Liver spots

Very frequent (80-99%)HP:0001003

Multiple cafe-au-lait spots

Very frequent (80-99%)HP:0007565

Near sighted

Very frequent (80-99%)HP:0000545

Nevocellular nevi

Very frequent (80-99%)HP:0000995

Sore in the lining of gastrointestinal tract

Very frequent (80-99%)HP:0004398

Stomach hernia

Very frequent (80-99%)HP:0002036

Flat nasal bridge

Frequent (30-79%)HP:0005280

NIDDM

Frequent (30-79%)HP:0005978

Mongoloid slant

Occasional (5-29%)HP:0000582

Plaque build-up in arteries supplying blood to heart

Occasional (5-29%)HP:0001677

Squint

Occasional (5-29%)HP:0000486

Unibrow

Occasional (5-29%)HP:0000664

Flat light-brown mark on skin

HP:0000957

Related Conditions

Autosomal dominant hereditary disorder(parent)

Digestive system hereditary disorder(parent)

Genetic disorder of skin pigmentation(parent)

Hyperpigmentation of skin(parent)

Disorder of upper gastrointestinal tract(parent)

Hereditary disorder of the integument(parent)

Quick Facts

SNOMED CT: 782946000
UMLS CUI: C1850899
Fully Specified Name: Gastrocutaneous syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.