EC23.1 Syndromic genetically-determined hypermelanosis or lentiginosis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
code elsewhere
- 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)
synonyms
- Syndromic genetically-determined hypermelanosis or lentiginosis
- Gastrocutaneous syndrome
- Watson syndrome
- Café-au-lait macules with pulmonary stenosis (MIM 193520)
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