Rombo syndrome

disorder

SNOMED 721904001CUI C1867147

Overview

Rombo 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.

Abnormality of the eyebrow

HP:0000534

Abnormality of the eyelashes

HP:0000499

Basal cell nevus

HP:0002671

Facial telangiectasia

HP:0007380

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hypotrichosis(parent)

Hereditary disorder of the integument(parent)

Hereditary neoplastic syndrome(parent)

Atrophic condition of skin(parent)

Quick Facts

SNOMED CT: 721904001
UMLS CUI: C1867147
Fully Specified Name: Rombo syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 4

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.