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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 EDAR 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)
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last database update
MGI 6.20
The Jackson Laboratory