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80902009: Neutral 1 amino acid transport defect (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
134190018 Neutral 1 amino acid transport defect en Synonym Active Entire term case insensitive SNOMED CT core module
134191019 Hartnup disease en Synonym Active Entire term case sensitive SNOMED CT core module
134192014 Hartnup disorder en Synonym Active Entire term case sensitive SNOMED CT core module
822114012 Neutral 1 amino acid transport defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1234522018 Neutral amino acid transport defect en Synonym Active Entire term case insensitive SNOMED CT core module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neutral 1 amino acid transport defect Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Neutral 1 amino acid transport defect Is a Specific renal tubule transport defect true Inferred relationship Existential restriction modifier
Neutral 1 amino acid transport defect Is a Hereditary disorder of the urinary system false Inferred relationship Existential restriction modifier
Neutral 1 amino acid transport defect Is a Amino acid transport disorder true Inferred relationship Existential restriction modifier
Neutral 1 amino acid transport defect Occurrence Congenital false Inferred relationship Existential restriction modifier
Neutral 1 amino acid transport defect Finding site Kidney structure true Inferred relationship Existential restriction modifier 1
Neutral 1 amino acid transport defect Is a Metabolic renal disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hartnup disorder, renal type Is a True Neutral 1 amino acid transport defect Inferred relationship Existential restriction modifier
Hartnup disorder, renal/jejunal type Is a True Neutral 1 amino acid transport defect Inferred relationship Existential restriction modifier
Dystonia due to neutral 1 amino acid transport defect Due to True Neutral 1 amino acid transport defect Inferred relationship Existential restriction modifier 3

This concept is not in any reference sets

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