Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3725375014 | Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3725376010 | Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3725377018 | Nephrotic syndrome, hearing loss, pretibial epidermolysis bullosa syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Is a | Nephrotic syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Finding site | Glomerulus structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Is a | Auditory system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Finding site | Ear structure | true | Inferred relationship | Existential restriction modifier | 4 | |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Interprets | Hearing, function | true | Inferred relationship | Existential restriction modifier | 5 | |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Is a | Hereditary nephritis | true | Inferred relationship | Existential restriction modifier | ||
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Associated morphology | Chronic inflammation | true | Inferred relationship | Existential restriction modifier | 1 | |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Is a | Sensorineural hearing loss | true | Inferred relationship | Existential restriction modifier | ||
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier | 3 | |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Has interpretation | Above reference range | true | Inferred relationship | Existential restriction modifier | 2 | |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Interprets | Albumin measurement | true | Inferred relationship | Existential restriction modifier | 3 | |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Interprets | Measurement of protein in urine | true | Inferred relationship | Existential restriction modifier | 2 | |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome | Is a | Disorder of ear | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR