Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4669053017 | Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4669054011 | Cerebrorenal syndrome Perez type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4669055012 | Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | Chronic nervous system disorder | true | Inferred relationship | Existential restriction modifier | ||
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | Chronic metabolic disorder | true | Inferred relationship | Existential restriction modifier | ||
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | Oculomotor apraxia | true | Inferred relationship | Existential restriction modifier | ||
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Existential restriction modifier | ||
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | Disorder of zinc metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 2 | |
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Finding site | Structure of visual system | true | Inferred relationship | Existential restriction modifier | 3 | |
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Existential restriction modifier | 1 | |
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Finding site | Structure of central nervous system | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR