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


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

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 (core metadata concept) SNOMED CT core
3310254011 Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311717010 Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) Is a Familial hypomagnesemia-hypercalciuria true Inferred relationship Some
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) Is a Hereditary disorder of the urinary system true Inferred relationship Some
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) Finding site Urinary system structure (body structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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