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711151004: Hypomagnesemia with secondary hypocalcemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2015. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3047500019 Hypomagnesemia with secondary hypocalcemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3047501015 Hypomagnesemia with secondary hypocalcemia en Synonym Active Entire term case insensitive SNOMED CT core module
3047502010 Hypomagnesaemia with secondary hypocalcaemia en Synonym Active Entire term case insensitive SNOMED CT core module
3047504011 Intestinal hypomagnesemia 1 en Synonym Active Entire term case insensitive SNOMED CT core module
3047505012 Intestinal hypomagnesaemia 1 en Synonym Active Entire term case insensitive SNOMED CT core module
3047506013 Intestinal hypomagnesemia with secondary hypocalcemia en Synonym Active Entire term case insensitive SNOMED CT core module
3047507016 Intestinal hypomagnesaemia with secondary hypocalcaemia en Synonym Active Entire term case insensitive SNOMED CT core module
3047508014 Familial primary hypomagnesemia with hypocalcuria en Synonym Active Entire term case insensitive SNOMED CT core module
3047509018 Familial primary hypomagnesaemia with hypocalcuria en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypomagnesemia with secondary hypocalcemia Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Is a Parathyroid hypocalcemic tetany true Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Is a Primary hypomagnesemia true Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Finding site Parathyroid structure false Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier
Hypomagnesemia with secondary hypocalcemia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hypomagnesemia with secondary hypocalcemia Finding site Structure of nervous system true Inferred relationship Existential restriction modifier 1
Hypomagnesemia with secondary hypocalcemia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Hypomagnesemia with secondary hypocalcemia Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 2
Hypomagnesemia with secondary hypocalcemia Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 3
Hypomagnesemia with secondary hypocalcemia Has interpretation Decreased true Inferred relationship Existential restriction modifier 3
Hypomagnesemia with secondary hypocalcemia Is a Congenital disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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