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

703231005: Familial hyperaldosteronism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3007909011 Familial hyperaldosteronism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3007954012 Familial hyperaldosteronism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3007909011 Familial hyperaldosteronism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3007909011 Familial hyperaldosteronism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3007954012 Familial hyperaldosteronism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3007954012 Familial hyperaldosteronism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
872421000172118 FH - familial hyperaldosteronism fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
978701000172113 hyperaldostéronisme familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
872421000172118 FH - familial hyperaldosteronism fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
978701000172113 hyperaldostéronisme familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hyperaldosteronism Is a Primary hyperaldosteronism (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial hyperaldosteronism Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial hyperaldosteronism Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial hyperaldosteronism Is a Hereditary disorder of endocrine system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial hyperaldosteronism type 1 Is a True Familial hyperaldosteronism Inferred relationship Existential restriction modifier (core metadata concept)
Familial hyperaldosteronism type 2 Is a True Familial hyperaldosteronism Inferred relationship Existential restriction modifier (core metadata concept)
Familial hyperaldosteronism type 3 (disorder) Is a True Familial hyperaldosteronism Inferred relationship Existential restriction modifier (core metadata concept)
A rare familial hyperaldosteronism characterized by elevated aldosterone levels and low plasma renin activity, early-onset hypertension, and hypokalemia. Developmental delay, learning disabilities, behavioral abnormalities, and attention deficit disorder are observed in some patients. Is a True Familial hyperaldosteronism Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start