Search Ontology:
Human Disease

Ehlers-Danlos syndrome classic type 2

Term ID
DOID:0080726
Synonyms
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models