FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

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


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3310254011 Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement en Synonym Active Case insensitive SNOMED CT core
3311717010 Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start