Familial calcium pyrophosphate dihydrate crystal deposition disease

disorder

SNOMED 1162808000CUI C5700249

Overview

Familial calcium pyrophosphate dihydrate crystal deposition disease is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormality of the intervertebral disc

Very frequent (80-99%)HP:0005108

Arthritic pain

Very frequent (80-99%)HP:0002829

Arthritis

Very frequent (80-99%)HP:0001369

Calcification of cartilage

Very frequent (80-99%)HP:0100593

Joint swelling

Very frequent (80-99%)HP:0001386

Osteoarthritis

Frequent (30-79%)HP:0002758

Ankylosis

Occasional (5-29%)HP:0031013

Calcium deposits in joints

Occasional (5-29%)HP:0000934

Decreased BMI

Occasional (5-29%)HP:0045082

Decreased bone mineral density Z score

Occasional (5-29%)HP:0004349

Increased inflammatory response

Occasional (5-29%)HP:0012649

Joint dislocation

Occasional (5-29%)HP:0001373

Limitation of joint mobility

Occasional (5-29%)HP:0001376

Pyrexia

Occasional (5-29%)HP:0001945

Stiff joint

Occasional (5-29%)HP:0001387

Synovitis

Occasional (5-29%)HP:0100769

Seizures

Very rare (1-4%)HP:0001250

Related Conditions

Autosomal dominant hereditary disorder(parent)

CPPD - Calcium pyrophosphate deposition disease(parent)

Hereditary disorder of musculoskeletal system(parent)

Periarthritis(parent)

Quick Facts

SNOMED CT: 1162808000
UMLS CUI: C5700249
Fully Specified Name: Familial calcium pyrophosphate dihydrate crystal deposition disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 17

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.