Autosomal dominant hypophosphataemic bone disease

disorder

SNOMED 237890006CUI C0342644

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Autosomal dominant hypophosphatemic rickets(child)

Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis(child)

Hypophosphatemia(parent)

Dysplasia with defective mineralization(parent)

Hereditary disorder of musculoskeletal system(parent)

Autosomal dominant hereditary disorder(parent)

Metabolic bone disease(parent)

Lesion of bone(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 237890006
UMLS CUI: C0342644
Fully Specified Name: Autosomal dominant hypophosphatemic bone disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.