Overview
Genetic disorder of skin pigmentation is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Xeroderma pigmentosum(child)
Oculocutaneous albinism(child)
Kitamura's reticulate acropigmentation(child)
Legius syndrome(child)
Oculocerebral hypopigmentation syndrome of Preus type(child)
X-linked reticulate pigmentary disorder with systemic manifestation syndrome(child)
Piebaldism(child)
Vici syndrome(child)
Deaf blind hypopigmentation syndrome Yemenite type(child)
Osteoporosis and oculocutaneous hypopigmentation syndrome(child)
Neuroectodermal melanolysosomal disease(child)
Deafness, vitiligo, achalasia syndrome(child)
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome(child)
Carney complex(child)
Familial progressive hyperpigmentation and hypopigmentation of skin(child)
Waardenburg's syndrome(child)
Hereditary hypermelanosis(child)
Piebald trait with neurologic defects syndrome(child)
Gastrocutaneous syndrome(child)
FACES (facial dysmorphism, anorexia, cachexia, eye and skin anomalies) syndrome(child)
Quick Facts
- SNOMED CT
- 724839001
- UMLS CUI
- C4511304
- Fully Specified Name
- Genetic disorder of skin pigmentation (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.