Osteogenesis imperfecta type IV

disorder

SNOMED 205497004CUI C0268363

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.

Popcorn calcification

Occasional (5-29%)HP:6000871

Biconcave flattened vertebrae

HP:0003321

Bowing of limbs due to multiple fractures

HP:0003023

Bowing of thighbone at birth, straightening with time

HP:0005005

Cobb angle greater than ten degrees

HP:0002650

Decreased body height

HP:0004322

Decreased bone mineral density Z score

HP:0004349

Dentinogenesis imperfecta

HP:0000703

Extra bones within cranial sutures

HP:0002645

Grey sclerae

HP:0000592

Hunched back

HP:0002808

Hypoacusis

HP:0000365

Increased fracture rate

HP:0002757

Increased susceptibility to fractures

HP:0002659

Otosclerosis

HP:0000362

Related Conditions

Osteogenesis imperfecta, type IV B(child)

Osteogenesis imperfecta, type IV A(child)

Osteogenesis imperfecta(parent)

Quick Facts

SNOMED CT: 205497004
UMLS CUI: C0268363
Fully Specified Name: Osteogenesis imperfecta type IV (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.