FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

80599001: Isolated corticotropin 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
133722015 Isolated corticotropin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
133723013 Specific corticotropin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
133724019 Isolated ACTH deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
821776013 Isolated corticotropin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated corticotropin deficiency est un(e) (attribut) Adrenocorticotropic hormone deficiency (disorder) true Inferred relationship Some
Isolated corticotropin deficiency localisation d'une constatation (attribut) Structure of pars distalis of pituitary (body structure) true Inferred relationship Some 1
Isolated corticotropin deficiency localisation d'une constatation (attribut) Entire endocrine gonad (body structure) false Inferred relationship Some
Isolated corticotropin deficiency localisation d'une constatation (attribut) glande suprarénale true Inferred relationship Some 2
Isolated corticotropin deficiency localisation d'une constatation (attribut) Pars anterior of pituitary gland false Inferred relationship Some
Isolated corticotropin deficiency interprète (attribut) Nutritional deficiency state false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital isolated adrenocorticotropic hormone deficiency (disorder) est un(e) (attribut) True Isolated corticotropin deficiency Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start