Polydactyly myopia syndrome

disorder

SNOMED 733087007CUI C1868117

Overview

Polydactyly myopia 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.

Near sighted

Very frequent (80-99%)HP:0000545

Postaxial hand polydactyly

Very frequent (80-99%)HP:0001162

Cryptorchidism

Frequent (30-79%)HP:0000028

Femoral hernia

Frequent (30-79%)HP:0100541

Inguinal hernia

Frequent (30-79%)HP:0000023

Related Conditions

Autosomal dominant hereditary disorder(parent)

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

Myopia(parent)

Hereditary disorder of the visual system(parent)

Accessory digit(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 733087007
UMLS CUI: C1868117
Fully Specified Name: Polydactyly myopia syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.