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721840000: syndroom van hyperurikemie, anemie en nierfalen (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3326212015 Hyperuricemia, anemia, renal failure syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326213013 Hyperuricemia, anemia, renal failure syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326214019 Hyperuricaemia, anaemia, renal failure syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326215018 Familial juvenile hyperuricemic nephropathy type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326216017 Familial juvenile hyperuricaemic nephropathy type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326217014 Renin associated familial juvenile hyperuricemic nephropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326218016 Renin associated familial juvenile hyperuricaemic nephropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6981771000146113 syndroom van hyperurikemie, anemie en nierfalen (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6981781000146110 syndroom van hyperurikemie, anemie en nierfalen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6981821000146115 syndroom van hyperurikemie, bloedarmoede en nierinsufficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3326219012 A rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326220018 A rare autosomal dominantly inherited disease of childhood characterised by hypoproliferative anaemia, hyperuricaemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Hyperuricemia true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Renal tubular disorder true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Urate nephropathy true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Hereditary nephropathy (disorder) true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Finding site Renal tubule structure (body structure) true Inferred relationship Some 1
Hyperuricemia, anemia, renal failure syndrome (disorder) Finding site Kidney structure false Inferred relationship Some 2
Hyperuricemia, anemia, renal failure syndrome (disorder) Causative agent Urate false Inferred relationship Some 2
Hyperuricemia, anemia, renal failure syndrome (disorder) Causative agent Urate true Inferred relationship Some 1
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Hereditary metabolic disease false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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