Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome

disorder

SNOMED 773300008CUI C1866728

Overview

Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of the integument(parent)

Spondyloepimetaphyseal disorder(parent)

Congenital hypotrichia(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Rhizomelic dysplasia(parent)

Quick Facts

SNOMED CT: 773300008
UMLS CUI: C1866728
Fully Specified Name: Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome (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.