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Disease Ontology Browser
adermatoglyphia (DOID:0111357)
Alliance: disease page
Synonyms: Absence of fingerprints; ADERM; ADG; Congenital absence of fingerprints; Immigration delay disease; Isolated congenital adermatoglyphia
Alt IDs: OMIM:136000, ORDO:289465
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory