OBO ID: DOID:0111010
Term Name: cone-rod dystrophy 5 Search Ontology:
Synonyms:
  • CORD5
Definition: A cone-rod dystrophy that has_material_basis_in mutation in the PITPNM3 gene in chromosome region 17p13.2-p13.1. https://www.ncbi.nlm.nih.gov/pubmed/17377520
References:
Ontology: Human Disease   ( DOID:0111010 )
Relationships
is a type of:
OTHER cone-rod dystrophy 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PITPNM3 Cone-rod dystrophy 5 600977
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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