Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 96816010 | Infantile neuronal ceroid lipofuscinosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 96817018 | Hagberg-Santavuori disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 96818011 | Santavuori disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 96819015 | Neuronal ceroid lipofuscinosis, infantile Finnish type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 96820014 | Polyunsaturated acid lipidosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 796970016 | Infantile neuronal ceroid lipofuscinosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1231818019 | Hagberg-Santavouri type neuronal ceroid lipofuscinosis | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1231819010 | Neuronal ceroid lipofuscinosis infantile Finnish type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1231820016 | Polyunsaturated fatty acid lipidosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1231821017 | Haltia-Santavouri type neuronal ceroid lipofuscinosis | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Infantile neuronal ceroid lipofuscinosis | Is a | Neuronal ceroid lipofuscinosis | true | Inferred relationship | Existential restriction modifier | ||
| Infantile neuronal ceroid lipofuscinosis | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Infantile neuronal ceroid lipofuscinosis | Associated morphology | Dystrophy | false | Inferred relationship | Existential restriction modifier | ||
| Infantile neuronal ceroid lipofuscinosis | Associated morphology | Degeneration | false | Inferred relationship | Existential restriction modifier | 1 | |
| Infantile neuronal ceroid lipofuscinosis | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 3 | |
| Infantile neuronal ceroid lipofuscinosis | Associated morphology | Degenerative abnormality | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Late-infantile neuronal ceroid lipofuscinosis | Is a | True | Infantile neuronal ceroid lipofuscinosis | Inferred relationship | Existential restriction modifier | |
| Progressive myoclonic epilepsy type 3 | Is a | True | Infantile neuronal ceroid lipofuscinosis | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR