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 |
5048286011 | Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5048287019 | Palmoplantar keratoderma, Charcot-Marie-Tooth syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5048291012 | Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5399980015 | A rare, genetic, autosomal dominant hereditary axonal motor and sensory neuropathy disorder characterized by childhood-onset palmoplantar keratoderma associated with motor and sensory polyneuropathy manifesting with late-onset, predominantly distal, lower limb muscle weakness and atrophy (later associating mild proximal weakness and upper limb involvement), moderate sensory impairment (hypoesthesia with stocking-glove distribution), and normal or near-normal nerve conduction velocities. Additional variable manifestations include impaired vibratory sensation, reduced tendon reflexes, paresthesia, pain, talipes equinovarus, pes cavus, and nail dystrophy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399981016 | A rare, genetic, autosomal dominant hereditary axonal motor and sensory neuropathy disorder characterised by childhood-onset palmoplantar keratoderma associated with motor and sensory polyneuropathy manifesting with late-onset, predominantly distal, lower limb muscle weakness and atrophy (later associating mild proximal weakness and upper limb involvement), moderate sensory impairment (hypoaesthesia with stocking-glove distribution), and normal or near-normal nerve conduction velocities. Additional variable manifestations include impaired vibratory sensation, reduced tendon reflexes, paraesthesia, pain, talipes equinovarus, pes cavus, and nail dystrophy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | Is a | Hereditary palmoplantar keratoderma | true | Inferred relationship | Some | ||
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | Is a | Hereditary motor and sensory neuropathy (disorder) | true | Inferred relationship | Some | ||
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | Finding site | Peripheral nervous system structure | true | Inferred relationship | Some | 3 | |
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | Finding site | Skin structure of sole of foot (body structure) | true | Inferred relationship | Some | 1 | |
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 2 | |
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)