Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies

disorder

SNOMED 1208985003CUI C5680313

Overview

Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies is a disorder.

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

Related Conditions

Congenital deficiency of pigment of skin(parent)

Multiple malformation syndrome with facial-limb defects as major feature(parent)

Ectodermal dysplasia with hair-tooth defects(parent)

Congenital hypotrichia(parent)

Genetic disorder of skin pigmentation(parent)

Quick Facts

SNOMED CT: 1208985003
UMLS CUI: C5680313
Fully Specified Name: Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies (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.