Search Ontology:
Human Disease

Ehlers-Danlos syndrome periodontal type 2

Term ID
DOID:0080987
Synonyms
Definition
An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the C1S gene on chromosome 12p13. https://pubmed.ncbi.nlm.nih.gov/27745832/
References
Ontology
Human Disease   ( DOID:0080987 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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