Juvenile polyposis of infancy

disorder

SNOMED 1156799009CUI C5445164

Overview

Juvenile polyposis of infancy 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.

Multiple colonic adenomatous polyps

Always present (100%)HP:0005227

Diarrhea

Very frequent (80-99%)HP:0002014

Gastrointestinal haemorrhage

Very frequent (80-99%)HP:0002239

Low number of red blood cells or haemoglobin

Very frequent (80-99%)HP:0001903

Black faeces

Frequent (30-79%)HP:0002249

Bleeding tendency

Frequent (30-79%)HP:0001892

Cachexia

Frequent (30-79%)HP:0004326

Gastrointestinal hamartomatous polyps

Frequent (30-79%)HP:0004390

Hemangiomata

Frequent (30-79%)HP:0001028

Hematochezia

Frequent (30-79%)HP:0002573

Hypoalbuminaemia

Frequent (30-79%)HP:0003073

Increased distance between eyes

Frequent (30-79%)HP:0000316

Large forehead

Frequent (30-79%)HP:0002003

Large head

Frequent (30-79%)HP:0000256

Malformation of face

Frequent (30-79%)HP:0001999

Mental-retardation

Frequent (30-79%)HP:0001249

Protein-losing enteropathy

Frequent (30-79%)HP:0002243

Refractory anemia

Frequent (30-79%)HP:0005505

Upset stomach

Frequent (30-79%)HP:0002027

Atria septal defect

Occasional (5-29%)HP:0001631

Broad phalanx of the toes

Occasional (5-29%)HP:0010174

Broad thumbs

Occasional (5-29%)HP:0011304

Cardiac anomaly

Occasional (5-29%)HP:0001627

Clubbing of fingers

Occasional (5-29%)HP:0100759

Decreased body height

Occasional (5-29%)HP:0004322

Delayed motor milestones

Occasional (5-29%)HP:0001270

Down-slanting palpebral fissure

Occasional (5-29%)HP:0000494

Flat nasal bridge

Occasional (5-29%)HP:0005280

Freckled genitalia

Occasional (5-29%)HP:0030257

Frontal protuberance

Occasional (5-29%)HP:0002007

Related Conditions

Juvenile polyposis syndrome(parent)

Quick Facts

SNOMED CT: 1156799009
UMLS CUI: C5445164
Fully Specified Name: Juvenile polyposis of infancy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.