Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3757317014 | Autosomal recessive optic atrophy OPA7 type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3757318016 | Autosomal recessive optic atrophy OPA7 (optic atrophy type 7) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3757319012 | Autosomal recessive optic atrophy type 7 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3757320018 | Autosomal recessive optic atrophy type 7 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3757321019 | A rare syndromic hereditary optic neuropathy disorder with characteristics of early-onset severe progressive visual impairment, optic disc pallor and central scotoma, variably associated with dyschromatopsia, auditory neuropathy (for example mild progressive sensorineural hearing loss), sensorimotor axonal neuropathy and occasionally moderate hypertrophic cardiomyopathy. There is evidence the disease is caused by homozygous mutation in the TMEM126A gene on chromosome 11q1. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
10018281000172118 | atrophie optique autosomique récessive de type 7 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
5088011000172114 | autosomaal recessieve opticusatrofie type 7 | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
5088021000172116 | autosomaal recessieve atrofie van nervus opticus type 7 | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive optic atrophy type 7 (disorder) | Finding site | Optic nerve structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive optic atrophy type 7 (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive optic atrophy type 7 (disorder) | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive optic atrophy type 7 (disorder) | Is a | Hereditary optic atrophy | true | Inferred relationship | Some | ||
Autosomal recessive optic atrophy type 7 (disorder) | Is a | Mitochondrial cytopathy (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set