OBO ID: DOID:0111016
Term Name: cone-rod dystrophy 13 Search Ontology:
Synonyms:
  • CORD13
Definition: A cone-rod dystrophy that has_material_basis_in mutation in the RPGRIP1 gene on chromosome 14q11.2. https://www.ncbi.nlm.nih.gov/pubmed/12920076
References:
Ontology: Human Disease   ( DOID:0111016 )
Relationships
is a type of:
OTHER cone-rod dystrophy 13 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RPGRIP1 Cone-rod dystrophy 13 608194
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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