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236470002: Specific renal tubule transport defect (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
354470014 Specific renal tubule transport defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
625067018 Specific renal tubule transport defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


33 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Specific renal tubule transport defect est un(e) (attribut) Kidney disease true Inferred relationship Some
Specific renal tubule transport defect est un(e) (attribut) Structural and functional abnormalities of the kidney false Inferred relationship Some
Specific renal tubule transport defect localisation d'une constatation (attribut) structure d'un rein true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis Due to False Specific renal tubule transport defect Inferred relationship Some 3
rachitisme hypophosphatémique autosomique dominant Due to True Specific renal tubule transport defect Inferred relationship Some 3
Autosomal dominant hypophosphataemic bone disease Due to True Specific renal tubule transport defect Inferred relationship Some 3
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis Due to True Specific renal tubule transport defect Inferred relationship Some 4
Autosomal dominant hypophosphataemic bone disease est un(e) (attribut) False Specific renal tubule transport defect Inferred relationship Some
Familial methionine malabsorption est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Histidine transport defect est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Neutral 1 amino acid transport defect est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
alcalose hypokaliémique familiale de type Gullner est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Familial x-linked hypophosphatemic vitamin D refractory rickets est un(e) (attribut) False Specific renal tubule transport defect Inferred relationship Some
Iminoglycinuria est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Cystinuria est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Hypophosphataemic rickets with nephrotic-glycosuric dwarfism Due to True Specific renal tubule transport defect Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Due to False Specific renal tubule transport defect Inferred relationship Some 2
rachitisme hypophosphatémique autosomique dominant Due to False Specific renal tubule transport defect Inferred relationship Some 2
Familial x-linked hypophosphatemic vitamin D refractory rickets Due to True Specific renal tubule transport defect Inferred relationship Some 2
High renal threshold for glucose est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Isolated hypercystinuria est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Dibasic aminoaciduria est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Glycinuria est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Familial renal hypouricaemia est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some
Renal glycosuria est un(e) (attribut) True Specific renal tubule transport defect Inferred relationship Some

This concept is not in any reference sets

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