Progressive myositis ossificans

disorder

SNOMED 82725007CUI C0016037

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.

Ectopic bone formation

Always present (100%)HP:0011986

Elevated alkaline phosphatase

Always present (100%)HP:0003155

Limited neck mobility

Always present (100%)HP:0005986

Abnormal hallux morphology

Very frequent (80-99%)HP:0001844

Calcification of muscle tissue

Very frequent (80-99%)HP:0011987

Fused neck

Very frequent (80-99%)HP:0002949

Limitation of joint mobility

Very frequent (80-99%)HP:0001376

Osteochondroma

Very frequent (80-99%)HP:0030431

Short hallux

Very frequent (80-99%)HP:0010109

Spinal rigidity

Very frequent (80-99%)HP:0003306

Subcutaneous nodule

Very frequent (80-99%)HP:0001482

Vertebral anomalies

Very frequent (80-99%)HP:0003468

Abnormal formation of the hip

Frequent (30-79%)HP:0001385

Abnormality of the femoral neck

Frequent (30-79%)HP:0003367

Abnormality of the thumbs

Frequent (30-79%)HP:0001172

Absent/small big toe bone

Frequent (30-79%)HP:0010058

Clinodactyly

Frequent (30-79%)HP:0030084

Cobb angle greater than ten degrees

Frequent (30-79%)HP:0002650

Hair loss

Frequent (30-79%)HP:0001596

Hip pain

Frequent (30-79%)HP:0030838

Hypoacusis

Frequent (30-79%)HP:0000365

Increased susceptibility to fractures

Frequent (30-79%)HP:0002659

Respiratory function loss

Frequent (30-79%)HP:0002093

Deep venous thrombosis

Occasional (5-29%)HP:0002625

Enchondroma

Occasional (5-29%)HP:0030038

Fusion of joints

Occasional (5-29%)HP:0100240

Kidney stones

Occasional (5-29%)HP:0000787

Lymphatic obstruction

Occasional (5-29%)HP:0001004

Postnatal failure to thrive

Occasional (5-29%)HP:0001508

Basal ganglion calcification

Very rare (1-4%)HP:0002135

Related Conditions

Autosomal dominant hereditary disorder(parent)

Ectopic bone tissue, congenital(parent)

Hereditary disorder of musculoskeletal system(parent)

Muscular ossification(parent)

Degenerative disorder of musculoskeletal system(parent)

Lesion of skeletal muscle(parent)

Deposition in skeletal muscle(parent)

Quick Facts

SNOMED CT: 82725007
UMLS CUI: C0016037
Fully Specified Name: Progressive myositis ossificans (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.