Search Ontology:
Human Disease

retinitis pigmentosa 79

Term ID
DOID:0061108
Synonyms
  • RP79
Definition
A retinitis pigmentosa that has_material_basis_in heterozygous mutation in the HK1 gene on chromosome 10q22. https://pubmed.ncbi.nlm.nih.gov/25190649/
References
Ontology
Human Disease   ( DOID:0061108 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
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