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45812003: Familial methionine malabsorption (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
1230267016 Oasthouse disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
76397018 Familial methionine malabsorption en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
76398011 Oast-house urine disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
76399015 Methionine malabsorption syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
76400010 Smith-Strang disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
76401014 Beery-baby syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
76402019 Oast-house disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
783093016 Familial methionine malabsorption (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial methionine malabsorption est un(e) (attribut) maladie métabolique du rein true Inferred relationship Some
Familial methionine malabsorption est un(e) (attribut) Specific renal tubule transport defect true Inferred relationship Some
Familial methionine malabsorption est un(e) (attribut) Hereditary disorder of the urinary system false Inferred relationship Some
Familial methionine malabsorption est un(e) (attribut) Disorder of sulphur-bearing amino acid metabolism true Inferred relationship Some
Familial methionine malabsorption est un(e) (attribut) Congenital anomaly of trunk false Inferred relationship Some
Familial methionine malabsorption localisation d'une constatation (attribut) structure d'un rein true Inferred relationship Some 1
Familial methionine malabsorption survenue (attribut) congénital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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