Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
377984017 | Nephronophthisis - medullary cystic disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
644698015 | Nephronophthisis - medullary cystic disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
6403651000241110 | néphronophtise-maladie kystique de la médullaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6403661000241113 | néphronophtise-maladie kystique de la médullaire rénale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Medullary cystic disease of the kidney | Is a | False | Nephronophthisis - medullary cystic disease | Inferred relationship | Some | |
Nephronophthisis | Is a | True | Nephronophthisis - medullary cystic disease | Inferred relationship | Some | |
A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia. | Is a | True | Nephronophthisis - medullary cystic disease | Inferred relationship | Some |
This concept is not in any reference sets