Gastrocutaneous syndrome

Orpha code: 2069OMIM code: 137270

Definicja

A rare, syndromic, hyperpigmentation of the skin characterized by multiple lentigines and café-au-lait spots associated with hiatal hernia and peptic ulcer, hypertelorism and myopia. There have been no further descriptions in the literature since 1982.

Disease data
Klasyfikacja

Disease

Kod ORPHA
2069
Kod OMIM
137270
Kod ICD10
-
Kod ICD11
EC23.1

No additional description.

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