FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

13003007: Cystathioninuria (disorder)


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
22267013 Cystathioninuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474888013 CTH - Cystathioninuria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
734247015 Cystathioninuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5144622010 Cystathionine gamma-lyase deficiency syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5144623017 A rare inborn error of metabolism with characteristics of abnormal accumulation of plasma cystathionine and subsequent increased urinary excretion due to cystathionine gamma-lyase deficiency. The condition is considered benign without pathological relevance. Mode of inheritance is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
22267013 Cystathioninuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
22267013 Cystathioninuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474888013 CTH - Cystathioninuria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
734247015 Cystathioninuria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
734247015 Cystathioninuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5144622010 Cystathionine gamma-lyase deficiency syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5144623017 A rare inborn error of metabolism with characteristics of abnormal accumulation of plasma cystathionine and subsequent increased urinary excretion due to cystathionine gamma-lyase deficiency. The condition is considered benign without pathological relevance. Mode of inheritance is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3410331001000116 Cystathioninurie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
934931000172113 déficit en cystathionase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1008421000172111 cystathioninurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
934931000172113 déficit en cystathionase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1008421000172111 cystathioninurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3410331001000116 Cystathioninurie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cystathioninuria Is a Disorder of sulphur-bearing amino acid metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Cystathioninuria Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Cystathioninuria Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Cystathioninuria Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Cystathioninuria Due to Cystathionine gamma-lyase deficiency true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cystathioninuria Is a Inborn error of amino acid metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Cystathioninuria Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start