Progressive osseous heteroplasia

disorder

SNOMED 719271000CUI C0334041

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.

Bone pain

Very frequent (80-99%)HP:0002653

Ectopic calcification

Very frequent (80-99%)HP:0010766

Limitation of joint mobility

Very frequent (80-99%)HP:0001376

Multiple, subcutaneous nodules

Very frequent (80-99%)HP:0001482

Calcification of muscle tissue

Frequent (30-79%)HP:0011987

Brachydactyly

Occasional (5-29%)HP:0001156

Cancer of connective tissue

Occasional (5-29%)HP:0100242

Flat, discolored area of skin

Occasional (5-29%)HP:0012733

Hyperpigmented macules

Occasional (5-29%)HP:0001034

Osteoarthritis

Occasional (5-29%)HP:0002758

Papules

Occasional (5-29%)HP:0200034

Parathyroid disease

Occasional (5-29%)HP:0000828

Ankylosis

HP:0031013

Osteoma cutis

HP:0025027

Short limbs

HP:0009826

Related Conditions

Autosomal dominant hereditary disorder(parent)

Ectopic bone tissue, congenital(parent)

Muscular ossification(parent)

Quick Facts

SNOMED CT: 719271000
UMLS CUI: C0334041
Fully Specified Name: Progressive osseous heteroplasia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.