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

1231283007: Congenital isolated adrenocorticotropic hormone deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5072045012 Congenital isolated adrenocorticotropic hormone deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5072046013 Congenital isolated adrenocorticotropic hormone deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5072047016 Congenital isolated ACTH (adrenocorticotropic hormone) deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5072048014 A rare endocrine disease characterised by neonatal hypoglycaemia, prolonged cholestatic jaundice, and seizures. Typical are low plasma adrenocorticotropic hormone (ACTH) and cortisol levels in the absence of structural pituitary defects. Low partial growth hormone deficiency is sometimes associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5072049018 A rare endocrine disease characterized by neonatal hypoglycemia, prolonged cholestatic jaundice, and seizures. Typical are low plasma adrenocorticotropic hormone (ACTH) and cortisol levels in the absence of structural pituitary defects. Low partial growth hormone deficiency is sometimes associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital isolated adrenocorticotropic hormone deficiency (disorder) est un(e) (attribut) Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
Congenital isolated adrenocorticotropic hormone deficiency (disorder) est un(e) (attribut) Hereditary disorder of nervous system true Inferred relationship Some
Congenital isolated adrenocorticotropic hormone deficiency (disorder) est un(e) (attribut) Congenital disease true Inferred relationship Some
Congenital isolated adrenocorticotropic hormone deficiency (disorder) est un(e) (attribut) Isolated corticotropin deficiency true Inferred relationship Some
Congenital isolated adrenocorticotropic hormone deficiency (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital isolated adrenocorticotropic hormone deficiency (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital isolated adrenocorticotropic hormone deficiency (disorder) localisation d'une constatation (attribut) glande suprarénale true Inferred relationship Some 1
Congenital isolated adrenocorticotropic hormone deficiency (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Congenital isolated adrenocorticotropic hormone deficiency (disorder) localisation d'une constatation (attribut) Structure of pars distalis of pituitary (body structure) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start