Search Ontology:
Human Disease

posterior polymorphous corneal dystrophy 2

Term ID
DOID:0110856
Synonyms
  • Ppcd2
Definition
A posterior polymorphous corneal dystrophy that has_material_basis_in heterozygous mutation in the COL8A2 gene on chromosome 1p34.3. https://www.ncbi.nlm.nih.gov/pubmed/11689488
References
Ontology
Human Disease   ( DOID:0110856 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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