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236467001: Acquired Fanconi syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
354466018 Acquired Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
354467010 Secondary Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
625064013 Acquired Fanconi syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
354466018 Acquired Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
354467010 Secondary Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
625064013 Acquired Fanconi syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6002211000241113 syndrome de Fanconi acquis fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6002211000241113 syndrome de Fanconi acquis fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acquired Fanconi syndrome Is a Infantile nephropathic cystinosis false Inferred relationship Existential restriction modifier (core metadata concept)
Acquired Fanconi syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Acquired Fanconi syndrome Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept)
Acquired Fanconi syndrome Finding site Structure of interstitial tissue of kidney false Inferred relationship Existential restriction modifier (core metadata concept)
Acquired Fanconi syndrome Is a Proximal renal tubular acidosis true Inferred relationship Existential restriction modifier (core metadata concept)
Acquired Fanconi syndrome Finding site Kidney structure false Inferred relationship Existential restriction modifier (core metadata concept)
Acquired Fanconi syndrome Occurrence Period of life between birth and death true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired Fanconi syndrome Finding site Proximal convoluted renal tubule structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired Fanconi syndrome Is a Fanconi syndrome true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Adult Fanconi syndrome Is a True Acquired Fanconi syndrome Inferred relationship Existential restriction modifier (core metadata concept)
A rare monoclonal gammopathy characterized by renal proximal tubule dysfunction secondary to monoclonal kappa light chain deposits in proximal tubular cells. Clinical presentation is with variable chronic kidney disease, low molecular weight proteinuria, aminoaciduria, hyperphosphaturia, uricosuria, bicarbonaturia, and non-diabetic glycosuria. Renal phosphate and urate wasting may cause hypophosphatemia and hypouricemia. Is a False Acquired Fanconi syndrome Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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