PomBase home

Disease association ontology term - MONDO:0007619 - isolated congenital adermatoglyphia

Term summary

ID
MONDO:0007619
Name
isolated congenital adermatoglyphia
Ontology or CV name
Disease association
Definition
Isolated congenital adermatoglyphia is a rare, genetic develomental 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.

Parents

Annotation

Disease association

MONDO:0007619 - isolated congenital adermatoglyphia

References:

Genes: