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Metadata
ID DOID:0110422
Name autosomal recessive pericentral pigmentary retinopathy
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
Xrefs

ICD10CM:H35.5

MIM:268060

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal recessive disease

Subclass Logical Relationships

has material basis in some autosomal recessive inheritance

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