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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 SMARCAD1 on chromosome 4q22.3.


Contributing Projects:
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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last database update
12/03/2019
MGI 6.14
The Jackson Laboratory