FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

238066006: Loss of single peroxisomal function (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
356848015 Loss of single peroxisomal function en Synonym Active Entire term case insensitive SNOMED CT core module
626897019 Loss of single peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

16 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Loss of single peroxisomal function Is a Disorder of peroxisomal function true Inferred relationship Existential restriction modifier
Loss of single peroxisomal function Finding site Body system structure false Inferred relationship Existential restriction modifier
Loss of single peroxisomal function Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Peroxisomal thiolase deficiency Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Bifunctional peroxisomal enzyme deficiency Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Glutaryl-coenzyme A oxidase deficiency Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Isolated dihydroxyacetone phosphate acyltransferase deficiency Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Isolated alkyldihydroxyacetone phosphate synthase deficiency Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Adrenoleukodystrophy Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Primary hyperoxaluria, type I Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Acatalasemia Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Leukoencephalopathy, dystonia, motor neuropathy syndrome Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Contiguous ABCD1 DXS1357E deletion syndrome Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Acyl-coenzyme A oxidase deficiency Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier
Fatty acyl-coenzyme A reductase 1 deficiency Is a True Loss of single peroxisomal function Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start