64235006: Ethanolaminosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\...

\Hereditary metabolic disease\Inborn error of metabolism\éthanolaminose

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\éthanolaminose

\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\éthanolaminose

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\éthanolaminose
\Metabolic disease\Disorder of organic acid metabolism (disorder)\Disorder of amino acid metabolism (disorder)\Disorder of amino acid and organic acid metabolism\éthanolaminose
\Metabolic disease\Enzymopathy\éthanolaminose

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

106778014 Ethanolaminosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

106779018 Ethanolamine kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

106780015 Ethanolaminuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

803606017 Ethanolaminosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

106778014 Ethanolaminosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

106778014 Ethanolaminosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

106779018 Ethanolamine kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

106779018 Ethanolamine kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

106780015 Ethanolaminuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

106780015 Ethanolaminuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

803606017 Ethanolaminosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

803606017 Ethanolaminosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6119971000241112 éthanolaminose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6119971000241112 éthanolaminose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
éthanolaminose	Is a	Disorder of amino acid and organic acid metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
éthanolaminose	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
éthanolaminose	Is a	Enzymopathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
éthanolaminose	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
éthanolaminose	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
éthanolaminose	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)