Hyperparathyroidism 2

disorder

SNOMED 702378002CUI C1704981

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.

Hypercalcemia

Always present (100%)HP:0003072

Parathyroid adenomas

Always present (100%)HP:0002897

Primary hyperparathyroidism

Always present (100%)HP:0008200

Abnormality of the parathyroid morphology

Very frequent (80-99%)HP:0011766

Hypercalciuria

Very frequent (80-99%)HP:0002150

Hypophosphataemia

Very frequent (80-99%)HP:0002148

Increased serum parathyroid hormone

Very frequent (80-99%)HP:0003165

Deglutition disorder

Frequent (30-79%)HP:0002015

Extreme thirst

Frequent (30-79%)HP:0001959

Fibroma

Frequent (30-79%)HP:0010614

Kidney stones

Frequent (30-79%)HP:0000787

Nephrocalcinosis

Frequent (30-79%)HP:0000121

Osteoporosis

Frequent (30-79%)HP:0000939

Shortened QT interval

Frequent (30-79%)HP:0012232

Tiredness

Frequent (30-79%)HP:0012378

Uterine fibroid

Frequent (30-79%)HP:0000131

Bone pain

Occasional (5-29%)HP:0002653

Calcium deposits in joints

Occasional (5-29%)HP:0000934

Constipation

Occasional (5-29%)HP:0002019

Headache

Occasional (5-29%)HP:0002315

Intermittent abdominal pain

Occasional (5-29%)HP:0002574

Lower jaw pain

Occasional (5-29%)HP:0200025

Muscle weakness

Occasional (5-29%)HP:0001324

Nausea and vomiting

Occasional (5-29%)HP:0002017

Pancreatitis

Occasional (5-29%)HP:0001733

Renal cyst

Occasional (5-29%)HP:0000107

Renal failure in adulthood

Occasional (5-29%)HP:0000083

Renal hamartoma

Occasional (5-29%)HP:0008696

Sore in the lining of gastrointestinal tract

Occasional (5-29%)HP:0004398

Fatty lump

Very rare (1-4%)HP:0012032

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of endocrine system(parent)

Familial hyperparathyroidism(parent)

Neoplasm of jaw(parent)

Quick Facts

SNOMED CT: 702378002
UMLS CUI: C1704981
Fully Specified Name: Hyperparathyroidism-jaw tumor 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.