Search Ontology:
Human Disease

X-linked cone-rod dystrophy 1

Term ID
DOID:0111008
Synonyms
  • COD1
  • CORDX1
  • X-linked cone dystrophy 1
Definition
A cone-rod dystrophy that has_material_basis_in mutation in an alternative terminal exon 15 of the RPGR gene on chromosome Xp11. https://www.ncbi.nlm.nih.gov/pubmed/11857109
References
Ontology
Human Disease   ( DOID:0111008 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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