Search Ontology:
Human Disease
Ehlers-Danlos syndrome classic type 2
- Term ID
- DOID:0080726
- Synonyms
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- Definition
- An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the collagen alpha-2(V) gene on chromosome 2q31 and that is characterized by the absence of widened atrophic scars. https://pubmed.ncbi.nlm.nih.gov/22696272/
- References
- Ontology
- Human Disease ( DOID:0080726 )
- is a type of
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Genes Involved
Zebrafish Models