Search Ontology:
Human Disease

cone-rod dystrophy 20

Term ID
DOID:0111026
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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