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DOID:0111357 - adermatoglyphia
Disease Ontology Definition: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.
Synonyms: Absence of fingerprints, ADERM, ADG, Congenital absence of fingerprints, Immigration delay disease, Isolated congenital adermatoglyphia
Xenbase Genes
:
smarcad1
| MIM:136000 - ADERMATOGLYPHIA; ADERM |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
skin disease (is_a)