Pseudocoxalgia

disorder

SNOMED 111255008CUI C1442965

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.

Arthritic pain

Very frequent (80-99%)HP:0002829

Cartilage destruction

Very frequent (80-99%)HP:0100773

Decreased body height

Very frequent (80-99%)HP:0004322

Delayed skeletal development

Very frequent (80-99%)HP:0002750

Joint dislocation

Very frequent (80-99%)HP:0001373

Neurogenic muscle atrophy, especially in the lower limbs

Very frequent (80-99%)HP:0003202

Osteochondronecrosis

Very frequent (80-99%)HP:0010885

Tooth abnormalities

Very frequent (80-99%)HP:0000164

Osteonecrosis of the femoral head

HP:0005743

Related Conditions

Avascular necrosis of head of femur(child)

Avascular necrosis of bone of hip(parent)

Injury of hip and thigh(parent)

Abnormality of epiphysis morphology of limb(parent)

Abnormality of long bone morphology(parent)

Quick Facts

SNOMED CT: 111255008
UMLS CUI: C1442965
Fully Specified Name: Avascular necrosis of capital femoral epiphysis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.