Search Ontology:
Human Disease

retinitis pigmentosa 42

Term ID
DOID:0110386
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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