FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

783620009: Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5408598018 A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408599014 A rare, genetic renal tubular disease characterised by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759533019 Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759536010 Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759537018 Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5591721000241115 hypophosphatémie dominante avec néphrolithiase et/ou ostéoporose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3440391001000112 Dominante Hypophosphatämie mit Nephrolithiasis oder Osteoporose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Finding site Osteoid tissue true Inferred relationship Some 1
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Associated morphology Dysplasia true Inferred relationship Some 1
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Is a Hereditary nephropathy (disorder) true Inferred relationship Some
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Is a Renal tubular disorder true Inferred relationship Some
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Is a Autosomal dominant hypophosphataemic bone disease true Inferred relationship Some
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Occurrence Congenital true Inferred relationship Some 1
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Due to Specific renal tubule transport defect false Inferred relationship Some 3
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Finding site Renal tubule structure false Inferred relationship Some 2
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Occurrence Congenital false Inferred relationship Some 4
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Pathological process (attribute) Pathological developmental process false Inferred relationship Some 4
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Associated morphology Impaired mineralization false Inferred relationship Some 4
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Finding site Bone structure false Inferred relationship Some 4
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Occurrence Congenital true Inferred relationship Some 3
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Associated morphology Impaired mineralization true Inferred relationship Some 2
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Finding site Bone structure true Inferred relationship Some 2
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Occurrence Congenital true Inferred relationship Some 2
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Finding site Renal tubule structure true Inferred relationship Some 3
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Due to Specific renal tubule transport defect true Inferred relationship Some 4
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Is a Urinary complication true Inferred relationship Some
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Is a Metabolic renal disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start