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GTR Home > Conditions/Phenotypes > Adermatoglyphia

Adermatoglyphia

Synonyms
FINGERPRINTS, ABSENCE OF; Isolated congenital adermatoglyphia
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

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. [from ORDO]

Available tests

6 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (6 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ADERM, BASNS, ETL1, HEL1, HRZ, TYS, SMARCAD1
    Summary: SNF2 related chromatin remodeling ATPase with DExD box 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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