OBO ID: DOID:0111026
Term Name: cone-rod dystrophy 20 Search Ontology:
Synonyms:
  • CORD20
Definition: A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the POC1B gene on chromosome 12q21. (2)
References:
Ontology: Human Disease   ( DOID:0111026 )
Relationships
is a type of:
OTHER cone-rod dystrophy 20 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
POC1B Cone-rod dystrophy 20 615973
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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