OBO ID: DOID:0110422
Term Name: autosomal recessive pericentral pigmentary retinopathy Search Ontology:
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)
OTHER autosomal recessive pericentral pigmentary retinopathy PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None