OBO ID: DOID:0111020
Term Name: cone-rod dystrophy 9 Search Ontology:
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 cone-rod dystrophy 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ADAM9 Cone-rod dystrophy 9 612775
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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