About   Help   FAQ
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.


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/12/2024
MGI 6.23
The Jackson Laboratory