FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

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


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
61539016 Hartnup disorder, renal/jejunal type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
768695018 Hartnup disorder, renal/jejunal type (disorder) en Fully specified name 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
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 (disorder) false Inferred relationship Some
Hartnup disorder, renal/jejunal type Is a Digestive system hereditary disorder (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
Hartnup disorder, renal/jejunal type Is a Disorder of jejunum (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start