Search Ontology:
Human Disease

cone-rod dystrophy 3

Term ID
DOID:0111013
Synonyms
  • CORD3
Definition
A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ABCA4 gene on chromosome 1p22. https://www.ncbi.nlm.nih.gov/pubmed/9466990
References
Ontology
Human Disease   ( DOID:0111013 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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