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36891003: Hartnup disorder, renal/jejunal type (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
61539016 Hartnup disorder, renal/jejunal type en Synonym Active Case sensitive SNOMED CT core
768695018 Hartnup disorder, renal/jejunal type (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hartnup disorder, renal/jejunal type Is a Disorder of jejunum true Inferred relationship Some
Hartnup disorder, renal/jejunal type Is a Congenital anomaly of digestive system false Inferred relationship Some
Hartnup disorder, renal/jejunal type Is a Neutral 1 amino acid transport defect true Inferred relationship Some
Hartnup disorder, renal/jejunal type Is a Disorder of small intestine false Inferred relationship Some
Hartnup disorder, renal/jejunal type Is a Disorder of lower gastrointestinal tract false Inferred relationship Some
Hartnup disorder, renal/jejunal type Is a Digestive system hereditary disorder false Inferred relationship Some
Hartnup disorder, renal/jejunal type Finding site Kidney structure true Inferred relationship Some 2
Hartnup disorder, renal/jejunal type Occurrence Congenital false Inferred relationship Some
Hartnup disorder, renal/jejunal type Finding site Jejunal 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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