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Disease Ontology Browser
ectodermal dysplasia 13 (DOID:0111650)
Alliance: disease page
Synonyms: ECTD13; ectodermal dysplasia 13, hair/tooth type
Alt IDs: OMIM:617392
Definition: An ectodermal dysplasia characterized by severe oligodontia accompanied by anomalies of hair and skin that has_material_basis_in homozygous or compound heterozygous mutation in KREMEN1 on chromosome 22q12.1.


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
06/23/2022
MGI 6.20
The Jackson Laboratory