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Human Disease

autosomal recessive pericentral pigmentary retinopathy

Term ID
DOID:0110422
Synonyms
Definition
A retinitis pigmentosa that is characterized autosomal recessive inheritance of pigmentary retinal degeneration with onset in the infancy but slower rates of progression than other forms of retinopathy. https://www.ncbi.nlm.nih.gov/pubmed/3189470
References
Ontology
Human Disease   ( DOID:0110422 )
Relationships
is a type of
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Genes Involved
Zebrafish Models