OBO ID: DOID:0111018
Term Name: cone-rod dystrophy 11 Search Ontology:
Synonyms:
  • CORD11
Definition: A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the RAX2 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/25789692
References:
Ontology: Human Disease   ( DOID:0111018 )
Relationships
is a type of:
OTHER cone-rod dystrophy 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RAX2 Cone-rod dystrophy 11
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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