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721840000: Hyperuricemia, anemia, renal failure syndrome (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3326213013 Hyperuricemia, anemia, renal failure syndrome en Synonym Active Case insensitive SNOMED CT core
3326214019 Hyperuricaemia, anaemia, renal failure syndrome en Synonym Active Case insensitive SNOMED CT core
3326215018 Familial juvenile hyperuricemic nephropathy type 2 en Synonym Active Case insensitive SNOMED CT core
3326216017 Familial juvenile hyperuricaemic nephropathy type 2 en Synonym Active Case insensitive SNOMED CT core
3326217014 Renin associated familial juvenile hyperuricemic nephropathy en Synonym Active Case insensitive SNOMED CT core
3326218016 Renin associated familial juvenile hyperuricaemic nephropathy en Synonym Active Case insensitive SNOMED CT core
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 Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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