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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