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Disease Ontology Browser
autosomal recessive type IV Ehlers-Danlos syndrome (DOID:14759)
Alliance: disease page
Synonyms: Ehlers-Danlos syndrome, recessive type 4
Alt IDs: UMLS_CUI:C0268340
Definition: An Ehlers-Danlos syndrome that is characterized by the association of unexpected organ fragility (arterial/bowel/gravid uterine rupture) with inconstant physical features as thin, translucent skin, easy bruising and acrogeric traits.


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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
02/20/2024
MGI 6.23
The Jackson Laboratory