About   Help   FAQ
Disease Ontology Browser
ectodermal dysplasia 10B (DOID:0111665)
Alliance: disease page
Synonyms: ECTD10B; ectodermal dysplasia 10B, hypohidrotic/hair/nail type, autosomal recessive
Alt IDs: OMIM:224900
Definition: A hypohidrotic ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the EDAR gene on chromosome 2q13.

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
11/12/2024
MGI 6.24 		The Jackson Laboratory