FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

303093006: Non-ketotic hyperglycinemia L protein deficiency (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
445165012 Non-ketotic hyperglycinaemia L protein deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
445166013 Non-ketotic hyperglycinemia type IV en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
445167016 Non-ketotic hyperglycinaemia type IV en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
445168014 Non-ketotic hyperglycinemia L protein deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
699270010 Non-ketotic hyperglycinemia L protein deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
7410191000241116 hyperglycinémie non cétosique de type IV fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7410201000241119 hyperglycinémie non cétosique par déficit en protéine L fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-ketotic hyperglycinaemia L protein deficiency Is a Non-ketotic hyperglycinaemia true Inferred relationship Some
Non-ketotic hyperglycinaemia L protein deficiency Finding site Body system structure false Inferred relationship Some
Non-ketotic hyperglycinaemia L protein deficiency Occurrence Congenital false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start