360381004: Alkaptonuria (finding)

Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

476131011 Alkaptonuria en Synonym Active Entire term case insensitive SNOMED CT core module
476132016 Alcaptonuria en Synonym Inactive Only initial character case insensitive SNOMED CT core module
740123013 Alkaptonuria (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
2463751015 Alkaptonuria (finding) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Alkaptonuria	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Existential restriction modifier
Alkaptonuria	Is a	Aciduria	false	Inferred relationship	Existential restriction modifier
Alkaptonuria	Finding site	Urinary system structure	false	Inferred relationship	Existential restriction modifier
Alkaptonuria	Interprets	Contents of urine	false	Inferred relationship	Existential restriction modifier
Alkaptonuria	Due to	Homogentisate 1,2-dioxygenase deficiency	false	Inferred relationship	Existential restriction modifier	1
Alkaptonuria	Interprets	Evaluation of urine specimen	false	Inferred relationship	Existential restriction modifier	2
Alkaptonuria	Interprets	Urine observable	false	Inferred relationship	Existential restriction modifier	3

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Ochronosis due to alkaptonuria	Associated etiologic finding	False	Alkaptonuria	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets