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

80710001: Primary hypomagnesemia (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
133884011 Primary hypomagnesemia en Synonym Active Entire term case insensitive SNOMED CT core module
504496013 Primary hypomagnesaemia en Synonym Active Entire term case insensitive SNOMED CT core module
821900010 Primary hypomagnesemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

13 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary hypomagnesemia Is a Metabolic disorder of transport true Inferred relationship Existential restriction modifier
Primary hypomagnesemia Is a Hypomagnesemia true Inferred relationship Existential restriction modifier
Primary hypomagnesemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Isolated familial intestinal hypomagnesemia Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier
Familial hypokalemia-hypomagnesemia Is a False Primary hypomagnesemia Inferred relationship Existential restriction modifier
Isolated familial renal hypomagnesemia Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier
Familial hypomagnesemia-hypercalciuria Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier
Familial hypokalemic and hypomagnesemic tubulopathy Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier
Familial primary hypomagnesemia with normocalciuria Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier
Hypomagnesemia co-occurrent with normocalciuria Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier
Isolated autosomal dominant hypomagnesemia Glaudemans type Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier
Autosomal dominant primary hypomagnesemia with hypocalciuria Is a True Primary hypomagnesemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start