loading...| Preferred Name | Retinitis Pigmentosa | |
| Synonyms |
Rod cone Dystrophy|Pigmentary retinopathy|Chorioretinal heredodystrophy|Tapetoretinal degeneration |
|
| ID |
http://bioontology.org/projects/ontologies/birnlex#birnlex_12820 |
|
| abbrev | ||
| class_or_indiv |
true |
|
| definition |
* hereditary, progressive degeneration of the neuroepithelium of the retina characterized by night blindness and progressive contraction of the visual field. (MSH) * group of inherited abnormalities in the retina; characterized by night blindness, retinal atrophy, weakening of the retinal vessels, pigment clumping, and contraction of the visual field. (CSP) |
|
| external_id_urls |
http://www.nlm.nih.gov/cgi/mesh/2008/MB_cgi?field=uid&term=D012174 |
|
| external_ids |
umlsCUI:C0035334|meshUID:D012174 |
|
| label |
Retinitis Pigmentosa |
|
| mod_date |
2007-11-18 |
|
| preferred_label |
Retinitis Pigmentosa |
|
| prefixIRI |
birnlex_12820 |
|
| prefLabel |
Retinitis Pigmentosa |
|
| retired |
false |
|
| synonyms |
Rod cone Dystrophy|Pigmentary retinopathy|Chorioretinal heredodystrophy|Tapetoretinal degeneration |
|
| subClassOf |
http://bioontology.org/projects/ontologies/birnlex#birnlex_12799 |