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 |
Deficiency of mevalonate kinase | Is a | Deficiency of transferase | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Deficiency of mevalonate kinase | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier (core metadata concept) |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A rare, severe form of mevalonate kinase deficiency (MKD) characterised by dysmorphic features, failure to thrive, psychomotor delay, ocular involvement, hypotonia, progressive ataxia, myopathy, and recurrent inflammatory episodes. | Is a | True | Deficiency of mevalonate kinase | Inferred relationship | Existential restriction modifier (core metadata concept) | |
Hyperimmunoglobulinemia D with periodic fever (disorder) | Is a | True | Deficiency of mevalonate kinase | Inferred relationship | Existential restriction modifier (core metadata concept) |
This concept is not in any reference sets