Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3756553016 | Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3756554010 | Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Is a | Intellectual disability | true | Inferred relationship | Existential restriction modifier | ||
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Is a | Metabolic disorder of transport | true | Inferred relationship | Existential restriction modifier | ||
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 1 | |
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Is a | Inherited metabolic disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 2 | |
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Interprets | Intellectual ability | true | Inferred relationship | Existential restriction modifier | 3 | |
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 3 | |
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Interprets | Adaptation behavior | true | Inferred relationship | Existential restriction modifier | 4 | |
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets