|  Help  |  About  |  Contact Us

DO Term : autosomal recessive pericentral pigmentary retinopathy [DOID:0110422] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • 268060,
  • OMIM:268060,
  • ICD10CM:H35.5
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents