Human genes for adermatoglyphia
Adermatoglyphia [DOID:0111357]
A skin disease characterized by lack of epidermal ridges on the fingers, toes, palms and soles that has_material_basis_in heterozygous mutation in SMARCAD1 on chromosome 4q22.3.
Synonyms: adermatoglyphia, adermatoglyphias, DOID:0111357, Absence of fingerprints, ADERM ...