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

237687003: Isolated growth hormone deficiency - autosomal dominant (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
356231015 Autosomal dominant isolated somatotropin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356232010 Isolated growth hormone deficiency - autosomal dominant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626450013 Isolated growth hormone deficiency - autosomal dominant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
356231015 Autosomal dominant isolated somatotropin deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356231015 Autosomal dominant isolated somatotropin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356232010 Isolated growth hormone deficiency - autosomal dominant en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356232010 Isolated growth hormone deficiency - autosomal dominant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626450013 Isolated growth hormone deficiency - autosomal dominant (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
626450013 Isolated growth hormone deficiency - autosomal dominant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3395951001000114 Wachstumshormonmangel, isolierter, Typ II de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5942231000241119 déficit isolé en hormone de croissance de transmission autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5942241000241112 déficit isolé en GH (growth hormone) autosomique dominante fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5942231000241119 déficit isolé en hormone de croissance de transmission autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5942241000241112 déficit isolé en GH (growth hormone) autosomique dominante fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3395951001000114 Wachstumshormonmangel, isolierter, Typ II 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
Autosomal dominant isolated somatotropin deficiency Is a Isolated somatotropin deficiency true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant isolated somatotropin deficiency Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant isolated somatotropin deficiency Finding site Pars anterior of pituitary gland false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant isolated somatotropin deficiency Interprets Nutritional deficiency state false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant isolated somatotropin deficiency Finding site Structure of distal part of pituitary true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start