Overview
Congenital deficiency of pigment of skin is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Congenital oculocutaneous hypopigmentation(child)
Oculocerebral hypopigmentation syndrome of Preus type(child)
Piebaldism(child)
Deaf blind hypopigmentation syndrome Yemenite type(child)
Deafness, vitiligo, achalasia syndrome(child)
Waardenburg's syndrome(child)
Piebald trait with neurologic defects syndrome(child)
Phylloid hypomelanosis(child)
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies(child)
Hypopigmentation of skin(parent)
Congenital pigmentary skin anomalies(parent)
Quick Facts
- SNOMED CT
- 1953005
- UMLS CUI
- C0265981
- Fully Specified Name
- Congenital deficiency of pigment of skin (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.