Spondylocamptodactyly syndrome

disorder

SNOMED 716231009CUI C4274762

Overview

Spondylocamptodactyly 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.

Flattened vertebral bodies

Very frequent (80-99%)HP:0000926

Proximal interphalangeal finger joint contractures

Very frequent (80-99%)HP:0100490

Scoliosis

Very frequent (80-99%)HP:0002650

Related Conditions

Multiple malformation syndrome with limb defect as major feature(parent)

Spondylodysplastic group(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 716231009
UMLS CUI: C4274762
Fully Specified Name: Spondylocamptodactyly syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 3

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.