loading...| Preferred Name |
corneal dystrophy |
| Synonyms |
corneal dystrophy (disease) corneal dystrophy |
| Definitions |
Editor note: NCIT distinguishes between acquired and genetic The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value. |
| ID |
http://purl.obolibrary.org/obo/MONDO_0018102 |
| comment |
Editor note: NCIT distinguishes between acquired and genetic |
| closeMatch | |
| database_cross_reference |
NCIT:C34513 ICD9:371.5 SCTID:5587004 MedDRA:10011005 MESH:D003317 HP:0001131 UMLS:C0010036 DOID:2566 ICD9:371.50 Orphanet:34533 |
| definition |
The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value. |
| exactMatch |
http://purl.obolibrary.org/obo/DOID_2566 http://identifiers.org/snomedct/5587004 http://purl.obolibrary.org/obo/Orphanet_34533 http://identifiers.org/mesh/D003317 |
| has characteristic | |
| has_exact_synonym |
corneal dystrophy (disease) corneal dystrophy |
| IAO_0000589 |
corneal dystrophy (disease) |
| id |
MONDO:0018102 |
| in_subset |
http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders |
| label |
corneal dystrophy |
| notation |
MONDO:0018102 |
| prefLabel |
corneal dystrophy |
| treeView | |
| subClassOf |