← Back to Conditions

Hereditary benign intraepithelial dyskeratosis

disorder
SNOMED 400014002CUI C0265966

Overview

Hereditary benign intraepithelial dyskeratosis 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.

Photophobia
Occasional (5-29%)HP:0000613
Impaired vision
HP:0000505
Oral white plaque
HP:0002745
Red eyes
HP:0025337

Related Conditions

Hereditary disorder of the integument(parent)
Digestive system hereditary disorder(parent)
Autosomal dominant hereditary disorder(parent)
Skin lesion(parent)
Lesion of oral mucosa(parent)
Congenital anomaly of oral mucosa(parent)
Congenital anomaly of skin(parent)
Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT
400014002
UMLS CUI
C0265966
Fully Specified Name
Hereditary benign intraepithelial dyskeratosis (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.