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784373007: Beta-mercaptolactate cysteine disulfiduria (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3763840015 Beta-mercaptolactate cysteine disulfiduria (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3763841016 Ampola syndrome en Synonym Active Case sensitive SNOMED CT core
3763842011 Beta-mercaptolactate cysteine disulfiduria en Synonym Active Case insensitive SNOMED CT core
3763843018 An extremely rare disorder of methionine cycle and sulfur amino acid metabolism with characteristics of increased urine excretion of beta-mercaptolactate-cysteine disulfide (due to deficiency of mercaptopyruvate sulfurtransferase activity in erythrocytes), leading to a positive cyanide nitroprusside test. Association with intellectual disability, congenital lens dislocation, and behavioral abnormalities has been reported, however the causal link remains to be established. There have been no further descriptions in the literature since 1981. en Definition Active Case sensitive SNOMED CT core
3763844012 An extremely rare disorder of methionine cycle and sulphur amino acid metabolism with characteristics of increased urine excretion of beta-mercaptolactate-cysteine disulfide (due to deficiency of mercaptopyruvate sulfurtransferase activity in erythrocytes), leading to a positive cyanide nitroprusside test. Association with intellectual disability, congenital lens dislocation, and behavioural abnormalities has been reported, however the causal link remains to be established. There have been no further descriptions in the literature since 1981. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Beta-mercaptolactate cysteine disulfiduria Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Beta-mercaptolactate cysteine disulfiduria Is a Disorder of sulfur-bearing amino acid metabolism true Inferred relationship Some
Beta-mercaptolactate cysteine disulfiduria Due to Deficiency of 3-mercaptopyruvate sulfurtransferase true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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