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717787005: Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3310253017 Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3310254011 Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement en Synonym Active Entire term case insensitive SNOMED CT core module
3311717010 Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement 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
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement Is a Familial hypomagnesemia-hypercalciuria true Inferred relationship Existential restriction modifier
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement Is a Hereditary disorder of the urinary system true Inferred relationship Existential restriction modifier
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement Finding site Urinary system structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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