Search Ontology:
Human Disease

cone-rod dystrophy 10

Term ID
DOID:0111017
Synonyms
  • CORD10
Definition
A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22. https://www.ncbi.nlm.nih.gov/pubmed/16199541
References
Ontology
Human Disease   ( DOID:0111017 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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