Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome

disorder

SNOMED 771187008CUI C1859690

Overview

Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome 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.

Camptodactyly of feet

Very frequent (80-99%)HP:0001836

Coxa vara

Very frequent (80-99%)HP:0002812

Flat head of thigh bone

Very frequent (80-99%)HP:0008812

Increased lumbar lordosis

Very frequent (80-99%)HP:0002938

Knee osteoarthritis

Very frequent (80-99%)HP:0005086

Osteoarthritis of the elbow

Very frequent (80-99%)HP:0003940

Polyarticular arthropathy

Very frequent (80-99%)HP:0005195

Proximal interphalangeal finger joint contractures

Very frequent (80-99%)HP:0100490

Wrist swelling

Very frequent (80-99%)HP:0001225

Bone cyst

Frequent (30-79%)HP:0012062

Hypoplastic femoral neck

Frequent (30-79%)HP:0100864

Osteoporosis

Frequent (30-79%)HP:0000939

Mitral regurgitation, mild

Occasional (5-29%)HP:0001653

Mitral valve prolapse

Occasional (5-29%)HP:0001634

Pleurisy

Occasional (5-29%)HP:0002102

Swelling or irritation of membrane around heart

Occasional (5-29%)HP:0001701

Ascites

Very rare (1-4%)HP:0001541

Infantile sensorineural hearing impairment

Very rare (1-4%)HP:0008610

Nuclear cataract

Very rare (1-4%)HP:0100018

Arthritis

HP:0001369

Congenital finger contractures

HP:0005879

Constrictive pericarditis

HP:0002563

Disease of the joints

HP:0003040

Flattened head of long bone of foot

HP:0005194

Flattened metacarpal heads

HP:0011909

Generalised morning stiffness

HP:0005197

Synovial lining hyperplasia

HP:0005186

Wrist contracture

HP:0001239

Related Conditions

Polyarthropathy(parent)

Hereditary disorder of musculoskeletal system(parent)

Recessive hereditary disorder (autosomal)(parent)

Fixed flexion deformity finger(parent)

Abnormality of interphalangeal joint of hand morphology(parent)

Quick Facts

SNOMED CT: 771187008
UMLS CUI: C1859690
Fully Specified Name: Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 28

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.