Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Disorder of glutamine metabolism | Is a | Disorder of amino acid and organic acid metabolism | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Disorder of glutamine metabolism | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Disorder of glutamine metabolism | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier (core metadata concept) |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A rare genetic neurometabolic disease characterised by early neonatal refractory seizures, hypotonia, and respiratory failure. Brain imaging reveals simplified gyral pattern of the frontal lobes, white matter abnormalities, gliosis and volume loss in various brain regions, and vasogenic oedema. Serum glutamine levels are significantly elevated. Death occurs within weeks after birth. | Is a | True | Disorder of glutamine metabolism | Inferred relationship | Existential restriction modifier (core metadata concept) | |
Spastic ataxia, dysarthria due to glutaminase deficiency | Is a | True | Disorder of glutamine metabolism | Inferred relationship | Existential restriction modifier (core metadata concept) |
This concept is not in any reference sets