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Human Disease

retinitis pigmentosa 107

Term ID
DOID:0051098
Synonyms
Definition
A retinitis pigmentosa that is charaterized by onset of RP ranging from the second decade to the sixth decade of life, with affected individuals experiencing night blindness, constriction of peripheral vision, and reduced visual acuity and that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP20 gene on chromosome 16q21. (2)
References
Ontology
Human Disease   ( DOID:0051098 )
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Genes Involved
Zebrafish Models