Hunter McAlpine craniosynostosis syndrome

disorder

SNOMED 721227001CUI C1832408

Overview

Hunter McAlpine craniosynostosis 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.

Almond shaped eyes

HP:0007874

Craniosyostosis

HP:0001363

Decreased body height

HP:0004322

Downturned corners of mouth

HP:0002714

Narrow mouth

HP:0000160

Nonprogressive mental retardation

HP:0001249

Related Conditions

Autosomal dominant hereditary disorder(parent)

Craniosynostosis syndrome(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 721227001
UMLS CUI: C1832408
Fully Specified Name: Hunter McAlpine craniosynostosis 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.