ICD-11 classes
14 Diseases of the skin
Genetic and developmental disorders affecting the skin
EC23 — Genetic disorders of skin pigmentation
EC23.1 — Syndromic genetically-determined hypermelanosis or...
ICD-11 EC23.1 — Syndromic genetically-determined hypermelanosis or lentiginosis
The diagnosis has no description.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis with code EC23.1 contains 3 clarifying diagnoses:
- LD2D.0 — Peutz-Jeghers syndrome
- LD27.00 — Incontinentia pigmenti
- LD2D.1 — Neurofibromatoses
It contains 5 clarifying diagnoses.
The diagnosis is coded elsewhere:
The diagnosis is included in 9 other classes.
- Peutz-Jeghers syndrome (LD2D.0)
- Incontinentia pigmenti (LD27.00)
- Neurofibromatoses (LD2D.1)
- Arterial dissection - lentiginosis (BD50.Z)
- McCune-Albright syndrome (FB80.0)
- LEOPARD syndrome (LD2F.1Y)
- Carney complex (5A70.Y)
- Bannayan-Riley-Ruvalcaba syndrome (LD2D.Y)
- Legius syndrome (LD27.5)