loading...| Preferred Name |
inherited retinal dystrophy |
|
| Synonyms |
fundus dystrophy genetic retinal dystrophy hereditary retinal degeneration hereditary retinal dystrophy retinal dystrophy familial retinal dystrophy |
|
| Definitions |
An instance of retinal degeneration that is caused by an inherited modification of the individual's genome. Editor note: This class deliberately merges distinct concepts of RD and inherited RD in other ontologies, as we believe these the same |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0019118 |
|
| comment |
Editor note: This class deliberately merges distinct concepts of RD and inherited RD in other ontologies, as we believe these the same |
|
| closeMatch |
http://identifiers.org/snomedct/193417000 |
|
| conformsTo |
http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml |
|
| database_cross_reference |
HP:0000556 MESH:D058499 DOID:8500 SCTID:314407005 Orphanet:71862 NCIT:C35625 ICD9:362.7 UMLS:C0854723 NCIT:C35194 COHD:377270 UMLS:C0154860 SCTID:41799005 ICD9:362.70 COHD:380395 ICD9:362.72 ICD10:H35.50 ICD9:362.75 DOID:8501 MedDRA:10038857 ICD10:H35.5 |
|
| disease causes dysfunction of | ||
| disease has feature | ||
| exactMatch |
http://purl.obolibrary.org/obo/DOID_8501 http://identifiers.org/mesh/D058499 http://identifiers.org/meddra/10038857 http://purl.obolibrary.org/obo/DOID_8500 http://www.orpha.net/ORDO/Orphanet_71862 http://purl.obolibrary.org/obo/NCIT_C35625 http://linkedlifedata.com/resource/umls/id/C0154860 http://identifiers.org/snomedct/41799005 http://identifiers.org/snomedct/314407005 |
|
| has broad synonym |
fundus dystrophy |
|
| has exact synonym |
genetic retinal dystrophy hereditary retinal degeneration hereditary retinal dystrophy retinal dystrophy familial retinal dystrophy |
|
| id |
MONDO:0019118 |
|
| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
|
| label |
inherited retinal dystrophy |
|
| notation |
MONDO:0019118 |
|
| prefLabel |
inherited retinal dystrophy |
|
| textual definition |
An instance of retinal degeneration that is caused by an inherited modification of the individual's genome. |
|
| subClassOf |