Isolated congenital adermatoglyphia

Orpha code: 289465OMIM code: 136000

Definition

Isolated congenital adermatoglyphia is a rare, genetic developmental defect during embryogenesis disorder characterized by the lack of epidermal ridges on the palms and soles, resulting in the absence of fingerprints, with no other associated manifestations. It is associated with a reduced number of sweat gland openings and reduced transpiration of palms and soles.

Disease data
Classification

Disease

Synonyms
Congenital absence of fingerprints
Wrodzony brak linii papilarnych
Immigration delay disease
ORPHA code
289465
OMIM code
136000
ICD10 code
Q82.8
ICD11 code
-

No additional description.

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