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Juvenile polyposis syndrome

disorder
SNOMED 9273005CUI C0345893

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.

Juvenile colonic polyposis
Always present (100%)HP:0012198
Juvenile GI polyposis
Always present (100%)HP:0004784
Rectal polyposis
Always present (100%)HP:0100896
Intestinal polyp
Very frequent (80-99%)HP:0005266
Gastrointestinal hamartomatous polyps
Frequent (30-79%)HP:0004390
Low number of red blood cells or haemoglobin
Frequent (30-79%)HP:0001903
Multiple gastric polyps
Frequent (30-79%)HP:0004394
Small intestinal polyposis
Frequent (30-79%)HP:0030256
Stomach pain
Frequent (30-79%)HP:0002027
Chronic extreme exhaustion
Occasional (5-29%)HP:0012432
Clubbing of fingers
Occasional (5-29%)HP:0100759
Colon cancer
Occasional (5-29%)HP:0003003
Diarrhea
Occasional (5-29%)HP:0002014
Digital clubbing
Occasional (5-29%)HP:0001217
Duodenal cancer
Occasional (5-29%)HP:0006771
Dysmorphic facies
Occasional (5-29%)HP:0001999
Edema
Occasional (5-29%)HP:0000969
Gastric cancer
Occasional (5-29%)HP:0012126
Gastrointestinal haemorrhage
Occasional (5-29%)HP:0002239
GI tract tumour
Occasional (5-29%)HP:0007378
Growth deficiency
Occasional (5-29%)HP:0001510
Hamartomatous stomach polyps
Occasional (5-29%)HP:0004795
Hematochezia
Occasional (5-29%)HP:0002573
Hyperplasia of forehead
Occasional (5-29%)HP:0002003
Increased size of skull
Occasional (5-29%)HP:0000256
Intussusception
Occasional (5-29%)HP:0002576
Mental retardation, mild
Occasional (5-29%)HP:0001256
Poor weight gain
Occasional (5-29%)HP:0001508
Rectocele
Occasional (5-29%)HP:0100822
Rectum protrudes through anus
Occasional (5-29%)HP:0002035

Related Conditions

Juvenile polyposis syndrome with hereditary haemorrhagic telangiectasia(child)
Juvenile polyposis of infancy(child)
Hamartoma(parent)
Autosomal dominant hereditary disorder(parent)
Digestive system hereditary disorder(parent)
Polyp(parent)
Disorder of gastrointestinal tract(parent)

Quick Facts

SNOMED CT
9273005
UMLS CUI
C0345893
Fully Specified Name
Juvenile polyposis syndrome (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.