OBO ID: DOID:0110386
Term Name: retinitis pigmentosa 42 Search Ontology:
Synonyms:
  • RP42
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the KLHL7 gene on chromosome 7p15.3. https://www.ncbi.nlm.nih.gov/pubmed/19520207
References:
Ontology: Human Disease   ( DOID:0110386 )
Relationships
is a type of:
OTHER retinitis pigmentosa 42 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KLHL7 Retinitis pigmentosa 42 612943
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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