Search Ontology:
Human Disease

cone-rod dystrophy 2

Term ID
DOID:0111005
Synonyms
  • cone-rod retinal dystrophy 2
  • CORD2
  • CRD2
  • RCRD2
  • retinal cone-rod dystrophy 2
Definition
A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/9390563
References
Ontology
Human Disease   ( DOID:0111005 )
Relationships
is a type of
disjoint_from
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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