OBO ID: DOID:0111025
Term Name: cone-rod dystrophy 19 Search Ontology:
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 cone-rod dystrophy 19 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TTLL5 Cone-rod dystrophy 19 615860
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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