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11282001: Homocystinuria (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
19556013 Homocystinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
643881012 Homocystinuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homocystinuria localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Homocystinuria survenue (attribut) congénital false Inferred relationship Some
Homocystinuria est un(e) (attribut) Disorder of sulphur-bearing amino acid metabolism true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Homocystinuria vitamin B12-responsive type III est un(e) (attribut) True Homocystinuria Inferred relationship Some
Cystathionine beta-synthase deficiency est un(e) (attribut) False Homocystinuria Inferred relationship Some
Methylene tetrahydrofolate methyltransferase reductase deficiency AND homocystinuria (disorder) est un(e) (attribut) True Homocystinuria Inferred relationship Some
Inherited methylmalonic acidemia AND homocystinuria est un(e) (attribut) True Homocystinuria Inferred relationship Some
Homocystinuria without methylmalonic aciduria (disorder) est un(e) (attribut) True Homocystinuria Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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