DO_rare_slim has material basis in disease has basis in disease has location autosomal dominant disease adermatoglyphia A skin disease characterized by lack of epidermal ridges on the fingers, toes, palms and soles that has_material_basis_in heterozygous mutation in the SMARCAD1 gene on chromosome 4q22.3. ADERM ADG Absence of fingerprints disease_ontology DOID:0111357 GARD:12550 MIM:136000 Congenital absence of fingerprints Immigration delay disease ORDO:289465 Isolated congenital adermatoglyphia skin disease autosomal dominant inheritance gene foot hand