Search Ontology:
Human Disease

cone-rod dystrophy 9

Term ID
DOID:0111020
Synonyms
  • CORD9
Definition
A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ADAM9 gene on chromosome 8p11. https://www.ncbi.nlm.nih.gov/pubmed/19409519
References
Ontology
Human Disease   ( DOID:0111020 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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