Hereditary neurocutaneous malformation

Orpha code: 1062OMIM code: 106070

Definicja

A rare genetic vascular anomaly characterized by the presence of angiomatous lesions affecting the skin, brain, and spinal cord. Lesions of the central nervous system have a marked tendency to bleed. There have been no further descriptions in the literature since 1988.

Disease data
Klasyfikacja

Disease

Kod ORPHA
1062
Kod OMIM
106070
Kod ICD10
D18.0
Kod ICD11
-

No additional description.

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