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410050000: Clinical manifestation of carnosinase deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2465501012 Clinical manifestation of carnosinase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2471777017 Clinical manifestation of carnosinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
2477712013 Clinical manifestation of aminoacyl-histidine dipeptidase deficiency 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
Clinical manifestation of carnosinase deficiency Is a Clinical manifestation of enzyme deficiency true Inferred relationship Existential restriction modifier
Clinical manifestation of carnosinase deficiency Due to Deficiency of aminoacyl-histidine dipeptidase true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Carnosinuria Is a True Clinical manifestation of carnosinase deficiency Inferred relationship Existential restriction modifier
Carnosinemia Is a True Clinical manifestation of carnosinase deficiency Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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