Related Conditions
Congenital deficiency of pigment of skin(child)
Neuroectodermal melanolysosomal disease(child)
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome(child)
Familial progressive hyperpigmentation and hypopigmentation of skin(child)
Carney complex, trismus, pseudocamptodactyly syndrome(child)
Familial generalised lentiginosis(child)
Inherited cutaneous hyperpigmentation(child)
Patterson syndrome(child)
McCune Albright syndrome(child)
Birthmark(child)
Dermal melanocytic hamartoma(child)
Congenital anomaly of skin(parent)
Skin pigmentation disorder(parent)
Quick Facts
- SNOMED CT
- 205564003
- UMLS CUI
- C0009726
- Fully Specified Name
- Congenital pigmentary skin 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.