FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

236470002: Specific renal tubule transport defect (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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


30 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Specific renal tubule transport defect Is a Kidney disease true Inferred relationship Some
Specific renal tubule transport defect Is a Structural and functional abnormalities of the kidney false Inferred relationship Some
Specific renal tubule transport defect Finding site Kidney structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis Due to False Specific renal tubule transport defect Inferred relationship Some 3
Autosomal dominant hypophosphataemic rickets 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 hypophosphataemia with nephrolithiasis and/or osteoporosis Due to True Specific renal tubule transport defect Inferred relationship Some 4
Autosomal dominant hypophosphataemic bone disease Is a False Specific renal tubule transport defect Inferred relationship Some
Familial methionine malabsorption Is a True Specific renal tubule transport defect Inferred relationship Some
Histidine transport defect Is a True Specific renal tubule transport defect Inferred relationship Some
Neutral 1 amino acid transport defect Is a True Specific renal tubule transport defect Inferred relationship Some
Familial hypokalaemic alkalosis, Gullner type Is a True Specific renal tubule transport defect Inferred relationship Some
Familial x-linked hypophosphataemic vitamin D refractory rickets Is a False Specific renal tubule transport defect Inferred relationship Some
Iminoglycinuria Is a True Specific renal tubule transport defect Inferred relationship Some
Cystinuria Is a 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
Autosomal dominant hypophosphataemic rickets Due to False Specific renal tubule transport defect Inferred relationship Some 2
Familial x-linked hypophosphataemic vitamin D refractory rickets Due to True Specific renal tubule transport defect Inferred relationship Some 2
High renal threshold for glucose Is a True Specific renal tubule transport defect Inferred relationship Some
Isolated hypercystinuria Is a True Specific renal tubule transport defect Inferred relationship Some
Dibasic aminoaciduria Is a True Specific renal tubule transport defect Inferred relationship Some
Glycinuria Is a True Specific renal tubule transport defect Inferred relationship Some
Familial renal hypouricaemia Is a True Specific renal tubule transport defect Inferred relationship Some
Renal glycosuria Is a True Specific renal tubule transport defect Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start