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45414006: Glucocorticoid deficiency with achalasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
75713010 Glucocorticoid deficiency with achalasia en Synonym Active Entire term case insensitive SNOMED CT core module
75714016 Achalasia-addisonian syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
75715015 Allgrove syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
75716019 Triple A syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
75717011 Alacrimia-achalasia-addisonianism en Synonym Active Entire term case insensitive SNOMED CT core module
782651012 Glucocorticoid deficiency with achalasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glucocorticoid deficiency with achalasia Is a Adrenal cortical hypofunction false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Interprets Achalasia false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Is a Achalasia of esophagus false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Is a Hereditary disorder of endocrine system false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Finding site Cardioesophageal junction structure false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Has definitional manifestation Achalasia false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Is a Adrenal cortical hypofunction false Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Is a Congenital achalasia of esophagus true Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Glucocorticoid deficiency with achalasia Finding site Cardioesophageal junction structure true Inferred relationship Existential restriction modifier 2
Glucocorticoid deficiency with achalasia Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Glucocorticoid deficiency with achalasia Finding site Esophageal structure false Inferred relationship Existential restriction modifier 1
Glucocorticoid deficiency with achalasia Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Glucocorticoid deficiency with achalasia Interprets Motility true Inferred relationship Existential restriction modifier 1
Glucocorticoid deficiency with achalasia Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 3
Glucocorticoid deficiency with achalasia Finding site Thyroid structure true Inferred relationship Existential restriction modifier 4
Glucocorticoid deficiency with achalasia Is a Adrenocorticotropic hormone resistance syndrome true Inferred relationship Existential restriction modifier
Glucocorticoid deficiency with achalasia Occurrence Congenital true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group
Autonomic neuropathy due to Allgrove syndrome Due to True Glucocorticoid deficiency with achalasia Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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