OBO ID: DOID:0111019
Term Name: cone-rod dystrophy 12 Search Ontology:
Synonyms:
  • CORD12
Definition: A cone-rod dystrophy that has_material_basis_in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15. (3)
References:
Ontology: Human Disease   ( DOID:0111019 )
Relationships
is a type of:
OTHER cone-rod dystrophy 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PROM1 Cone-rod dystrophy 12 612657
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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