Ehlers-Danlos syndrome classic-like 1 Disease Ontology Browser

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Disease Ontology Browser

Ehlers-Danlos syndrome classic-like 1 (DOID:0080731)
Alliance: disease page
Alt IDs: OMIM:606408
Definition: An Ehlers-Danlos syndrome that is characterized by hyperextensible skin, hypermobile joints, and tissue fragility and that has_material_basis_in omozygous or heterozygous mutation in the tenascin-XB gene (TNXB) on chromosome 6p21.

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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