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363224005: Neonatal renal disorder (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
482364012 Neonatal renal disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
755024012 Neonatal renal disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
7432391000241111 affection rénale néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7432401000241114 maladie néonatale du rein fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7432411000241111 néphropathie en période néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal renal disorder Is a Neonatal disorder true Inferred relationship Some
Neonatal renal disorder Occurrence Neonatal true Inferred relationship Some 1
Neonatal renal disorder Is a Kidney disease true Inferred relationship Some
Neonatal renal disorder Finding site Kidney structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Newborn renal dysfunction Is a True Neonatal renal disorder Inferred relationship Some
Neonatal nephrocalcinosis Is a True Neonatal renal disorder Inferred relationship Some
Neonatal iminoglycinuria Is a True Neonatal renal disorder Inferred relationship Some
Neonatal haemorrhage of kidney Is a True Neonatal renal disorder Inferred relationship Some
A rare genetic disease characterized by the association of Fanconi syndrome and nephrocalcinosis in addition to neonatal hyperinsulinism and macrosomia. Patients display a phenotype of proximal tubulopathy characterized by generalized aminoaciduria, low molecular weight proteinuria, glycosuria, hyperphosphaturia and hypouricemia, and additional features not normally seen in Fanconi syndrome (apart from nephrocalcinosis), namely renal impairment, hypercalciuria with relative hypocalcemia, and hypermagnesemia. Is a True Neonatal renal disorder Inferred relationship Some

This concept is not in any reference sets

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