Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2981441013 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2981448019 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2981489016 | Inherited retinal dystrophy primarily involving retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2981441013 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2981441013 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2981448019 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2981448019 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2981489016 | Inherited retinal dystrophy primarily involving retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2981489016 | Inherited retinal dystrophy primarily involving retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
515521000274111 | Erbbedingte Netzhautdystrophie, retinales Pigmentepithel primär betroffen | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
599751000274114 | Hereditäre Retinadystrophie, retinales Pigmentepithel primär betroffen | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6315181000241119 | dystrophie rétinienne héréditaire impliquant principalement l'épithélium pigmentaire rétinien | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6315191000241117 | dystrophie héréditaire de la rétine impliquant principalement l'épithélium pigmentaire rétinien | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6315181000241119 | dystrophie rétinienne héréditaire impliquant principalement l'épithélium pigmentaire rétinien | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6315191000241117 | dystrophie héréditaire de la rétine impliquant principalement l'épithélium pigmentaire rétinien | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
515521000274111 | Erbbedingte Netzhautdystrophie, retinales Pigmentepithel primär betroffen | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
599751000274114 | Hereditäre Retinadystrophie, retinales Pigmentepithel primär betroffen | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Is a | Hereditary retinal dystrophy (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Finding site | Retinal structure | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Biallelic RPE65 mutation associated retinal dystrophy | Is a | True | Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Inferred relationship | Existential restriction modifier (core metadata concept) |
This concept is not in any reference sets