Search Ontology:
Human Disease

cone-rod dystrophy 19

Term ID
DOID:0111025
Synonyms
  • CORD19
Definition
A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the TTLL5 gene on chromosome 14q24. https://www.ncbi.nlm.nih.gov/pubmed/24791901
References
Ontology
Human Disease   ( DOID:0111025 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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