has material basis in germline mutation in SMARCAD1 autosomal dominant disease isolated congenital adermatoglyphia https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/adermatoglyphia SCTID:763748007 GARD:0012550 isolated congenital adermatoglyphia DOID:0111357 congenital absence of fingerprints OMIM:136000 absence of fingerprints Orphanet:289465 immigration delay disease MONDO:0007619 ADERM 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. MESH:C565010 adermatoglyphia UMLS:C1852150 ADG MEDGEN:338875 fingerprints, absence of hereditary skin disorder