Gastrocutaneous syndrome

Orpha code: 2069OMIM code: 137270

Definition

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
Classification

Disease

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

No additional description.

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