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

• ICD10CM:H35.5
• OMIM:268060

Ontology

Human Disease   ( DOID:0110422 )