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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
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 Only initial character case insensitive (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
4510121000241117 maladie de Hartnup, type rénal/jéjunal fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4510121000241117 maladie de Hartnup, type rénal/jéjunal fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


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 Existential restriction modifier (core metadata concept)
Hartnup disorder, renal/jejunal type Is a Neutral 1 amino acid transport defect true Inferred relationship Existential restriction modifier (core metadata concept)
Hartnup disorder, renal/jejunal type Is a Disorder of small intestine (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hartnup disorder, renal/jejunal type Is a Disease of lower gastrointestinal tract false Inferred relationship Existential restriction modifier (core metadata concept)
Hartnup disorder, renal/jejunal type Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hartnup disorder, renal/jejunal type Finding site Kidney structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hartnup disorder, renal/jejunal type Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hartnup disorder, renal/jejunal type Finding site Jejunal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hartnup disorder, renal/jejunal type Is a Disorder of jejunum true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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