Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5048588011 | Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5048589015 | Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5400020011 | A rare, genetic, autosomal recessive axonal hereditary motor and sensory neuropathy disease characterized by prenatal onset of a severe sensorimotor axonal polyneuropathy (reflected by reduced fetal movement and polyhydramnios), manifesting, at birth, with respiratory failure requiring mechanical ventilation, profound muscular hypotonia, rapidly progressing distal muscle weakness, and absent deep tendon reflexes, in the absence of contractures, leading to death before 8 months of age. Neuropathological findings show severe loss of large- and medium-sized myelinated fibers without signs of demyelination. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400021010 | A rare, genetic, autosomal recessive axonal hereditary motor and sensory neuropathy disease characterised by prenatal onset of a severe sensorimotor axonal polyneuropathy (reflected by reduced fetal movement and polyhydramnios), manifesting, at birth, with respiratory failure requiring mechanical ventilation, profound muscular hypotonia, rapidly progressing distal muscle weakness, and absent deep tendon reflexes, in the absence of contractures, leading to death before 8 months of age. Neuropathological findings show severe loss of large- and medium-sized myelinated fibres without signs of demyelination. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Peripheral axonal neuropathy | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Chronic nervous system disorder (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Mixed sensory-motor polyneuropathy | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Hereditary motor and sensory neuropathy (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 1 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Chronic disease of musculoskeletal system | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Decreased muscle tone (finding) | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Interprets | Muscle tone | true | Inferred relationship | Some | 4 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 4 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Occurrence | Neonatal | true | Inferred relationship | Some | 2 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 2 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Congenital anomaly of central nervous system | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Neonatal disorder | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Congenital polyneuropathy | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Myoneural disorder | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Is a | Poor muscle tone (finding) | true | Inferred relationship | Some | ||
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 3 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 5 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Finding site | Axon structure | true | Inferred relationship | Some | 5 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 5 | |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 5 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)