Singh Williams McAlister syndrome

disorder

SNOMED 723580007CUI C4509954

Overview

Singh Williams McAlister 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.

Hypoplastic fourth metacarpal

Very frequent (80-99%)HP:0010044

Osteolysis of patellae

Very frequent (80-99%)HP:0006378

Osteolysis of scaphoids

Very frequent (80-99%)HP:0006202

Osteolysis of talus

Very frequent (80-99%)HP:0008095

Prominent joints

Very frequent (80-99%)HP:0003037

Synovitis

Very frequent (80-99%)HP:0100769

Related Conditions

Longitudinal deficiency of metacarpal bone(parent)

Recessive hereditary disorder (autosomal)(parent)

Osteolysis(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Degenerative disorder of extremity(parent)

Abnormally short fourth metacarpal(parent)

Quick Facts

SNOMED CT: 723580007
UMLS CUI: C4509954
Fully Specified Name: Talo-patello-scaphoid osteolysis syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.