Search Ontology:
Human Disease

cone-rod dystrophy 5

Term ID
DOID:0111010
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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