Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3440760015 | 5-amino-4-imidazole carboxamide ribosiduria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3440761016 | 5-amino-4-imidazole carboxamide ribosiduria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3440763018 | ATIC (5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/imp cyclohydrolase) deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3780959012 | AICA (5-amino-4-imidazole carboxamide) ribosiduria | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403441014 | A rare and severe inborn metabolic disease characterized clinically by the association of severe-to-profound neurodevelopmental impairment, severe visual impairment, ante-postnatal growth impairment, severe scoliosis and, frequently, early-onset epilepsy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403442019 | A rare and severe inborn metabolic disease characterised clinically by the association of severe-to-profound neurodevelopmental impairment, severe visual impairment, ante-postnatal growth impairment, severe scoliosis and, frequently, early-onset epilepsy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Disorder of purine metabolism | true | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Multiple malformation syndrome with limb defect as major feature | true | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Congenital anomaly of limb | true | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Mental retardation | false | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Hereditary macular dystrophy | true | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Finding site | Limb structure | true | Inferred relationship | Some | 2 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 2 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Finding site | Macula lutea structure | false | Inferred relationship | Some | 2 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 3 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Finding site | Limb structure | false | Inferred relationship | Some | 3 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Congenital anomaly of macula | true | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Finding site | Macula lutea structure | true | Inferred relationship | Some | 1 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 3 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 4 | |
5-amino-4-imidazole carboxamide ribosiduria (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)