Pancreatic polypeptidoma

disorder

SNOMED 255039001CUI C0346407

Overview

Pancreatic polypeptidoma 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.

Cancer of the pancreas

Very frequent (80-99%)HP:0002894

Small intestine tumor

Very frequent (80-99%)HP:0100833

Abnormality of the abdomen

Frequent (30-79%)HP:0001438

Anorexia

Frequent (30-79%)HP:0002039

Decreased bowel sounds

Frequent (30-79%)HP:0030144

Diarrhea

Frequent (30-79%)HP:0002014

Dyschezia

Frequent (30-79%)HP:0002019

Enlarged liver

Frequent (30-79%)HP:0002240

Episodic abdominal pain

Frequent (30-79%)HP:0002574

Nausea and vomiting

Frequent (30-79%)HP:0002017

No appetite

Frequent (30-79%)HP:0004396

Weight loss

Frequent (30-79%)HP:0001824

Ascites

Occasional (5-29%)HP:0001541

Bowel obstruction

Occasional (5-29%)HP:0005214

Extrahepatic cholestasis

Occasional (5-29%)HP:0012334

Gallstones

Occasional (5-29%)HP:0001081

Gastrointestinal haemorrhage

Occasional (5-29%)HP:0002239

Impaired release of bile from liver

Occasional (5-29%)HP:0001406

Intermittent yellowing of skin

Occasional (5-29%)HP:0001046

Intestinal carcinoid

Occasional (5-29%)HP:0006723

Lack of bowel sounds

Occasional (5-29%)HP:0030145

Adrenocortical adenoma

Very rare (1-4%)HP:0008256

Cushing syndrome

Very rare (1-4%)HP:0003118

Elevated circulating growth hormone concentration

Very rare (1-4%)HP:0000845

Gonadotropin excess

Very rare (1-4%)HP:0000837

Hypercalcemia

Very rare (1-4%)HP:0003072

Parathyroid adenomas

Very rare (1-4%)HP:0002897

Pituitary adenoma

Very rare (1-4%)HP:0002893

Primary hyperparathyroidism

Very rare (1-4%)HP:0008200

Prolactin excess

Very rare (1-4%)HP:0000870

Related Conditions

Neuroendocrine tumor of pancreas(parent)

Malignant tumour of endocrine pancreas(parent)

Quick Facts

SNOMED CT: 255039001
UMLS CUI: C0346407
Fully Specified Name: Pancreatic polypeptidoma (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.