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 |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive optic atrophy type 7 (disorder) | localisation d'une constatation (attribut) | Optic nerve structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive optic atrophy type 7 (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive optic atrophy type 7 (disorder) | morphologie associée (attribut) | Primary atrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive optic atrophy type 7 (disorder) | est un(e) (attribut) | Hereditary optic atrophy | true | Inferred relationship | Some | ||
Autosomal recessive optic atrophy type 7 (disorder) | est un(e) (attribut) | Mitochondrial cytopathy | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)