Hereditary pheochromocytoma and paraganglioma

disorder

SNOMED 716857003CUI C4274332

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.

Adrenal pheochromocytoma

Very frequent (80-99%)HP:0006748

Extraadrenal pheochromocytoma

Very frequent (80-99%)HP:0006737

Paraganglioma

Very frequent (80-99%)HP:0002668

Cerebral hemorrhage

Frequent (30-79%)HP:0001342

Chest pain

Frequent (30-79%)HP:0100749

Dysphonia

Frequent (30-79%)HP:0001618

Elevated urinary dopamine

Frequent (30-79%)HP:0011979

Elevated urinary epinephrine level

Frequent (30-79%)HP:0003639

Elevated urinary norepinephrine level

Frequent (30-79%)HP:0003345

Episodic hyperhidrosis

Frequent (30-79%)HP:0001069

Episodic paroxysmal anxiety

Frequent (30-79%)HP:0000740

Flushing

Frequent (30-79%)HP:0031284

Hypercalcemia

Frequent (30-79%)HP:0003072

Hypertension associated with pheochromocytoma

Frequent (30-79%)HP:0002640

Hypertensive retinopathy

Frequent (30-79%)HP:0001095

Intermittent abdominal pain

Frequent (30-79%)HP:0002574

Nausea

Frequent (30-79%)HP:0002018

Paragangliomas, head and neck

Frequent (30-79%)HP:0002864

Paroxysmal vertigo

Frequent (30-79%)HP:0010532

Positive regitine blocking test

Frequent (30-79%)HP:0003574

Proteinuria

Frequent (30-79%)HP:0000093

Pulsatile tinnitus

Frequent (30-79%)HP:0008629

Recurrent paroxysmal headache

Frequent (30-79%)HP:0002331

Renal glomerular fibrosis

Frequent (30-79%)HP:0000096

Sinus tach

Frequent (30-79%)HP:0011703

Skipped heart beat

Frequent (30-79%)HP:0001962

Tiredness

Frequent (30-79%)HP:0012378

Weight loss

Frequent (30-79%)HP:0001824

Arachnoid hemangiomatosis

Occasional (5-29%)HP:0012222

Blood in urine

Occasional (5-29%)HP:0000790

Related Conditions

Autosomal dominant hereditary disorder(parent)

Paraganglioma(parent)

Phaeochromocytoma(parent)

Quick Facts

SNOMED CT: 716857003
UMLS CUI: C4274332
Fully Specified Name: Hereditary pheochromocytoma and paraganglioma (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.