Search Ontology:
Human Disease

retinitis pigmentosa 100

Term ID
DOID:0061298
Synonyms
Definition
A retinitis pigmentosa characterized by the onset of night blindness in childhood or young adulthood, followed by progressive visual field constriction and that has_material_basis_in compound heterozygous mutation in the TBC1D32 gene on chromosome 6q22. https://pubmed.ncbi.nlm.nih.gov/37768732/
References
Ontology
Human Disease   ( DOID:0061298 )
Relationships
Other Pages
Genes Involved
Zebrafish Models