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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Retinal dystrophy +     
Chorioretinal dystrophy  
Cone/cone-rod dystrophy +   
Congenital stationary night blindness +   
Macular dystrophy +   
Pattern dystrophy of the retina +   
Retinal dystrophy with early macular involvement  
Rod-cone dystrophy +   
An inherited retinal disease subtype in which the rod photoreceptors appear to be more severely affected than the cone photoreceptors. Typical presentation is with nyctalopia (due to rod dysfunction) followed by loss of mid-peripheral field of vision, which gradually extends and leaves many patients with a small central island of vision due to the preservation of macular cones.

Synonyms
Exact Synonyms: Retinitis pigmentosa
Alternate IDs: HP:0000547 ;   HP:0001127 ;   HP:0007635 ;   HP:0007645 ;   HP:0007742 ;   HP:0007816 ;   HP:0007826 ;   HP:0007927 ;   HP:0008036
Xrefs: MESH:D012174 ;   SNOMEDCT_US:28835009 ;   UMLS:C0035334
Definition Sources: https://orcid.org/0000-0002-0736-9199, PMID:20212494

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