FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

1222672002: 3-methylglutaconic aciduria type 9 (disorder)


Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5048445018 3-methylglutaconic aciduria, epilepsy, spasticity, severe intellectual disability syndrome en Synonym Active Case insensitive SNOMED CT core
5048446017 3-methylglutaconic aciduria type 9 en Synonym Active Case insensitive SNOMED CT core
5048447014 3-methylglutaconic aciduria type 9 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5048448016 A rare organic aciduria characterized by early onset of global developmental delay with severe intellectual disability, seizures and 3-methylglutaconic aciduria. Additional features are hypotonia, hyperactivity and aggressive behavior, optic atrophy or spasticity. Brain imaging may show generalized cerebral atrophy and white matter abnormalities. en Definition Active Case sensitive SNOMED CT core
5048449012 A rare organic aciduria characterised by early onset of global developmental delay with severe intellectual disability, seizures and 3-methylglutaconic aciduria. Additional features are hypotonia, hyperactivity and aggressive behaviour, optic atrophy or spasticity. Brain imaging may show generalised cerebral atrophy and white matter abnormalities. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
3-methylglutaconic aciduria type 9 Is a Global developmental delay true Inferred relationship Some
3-methylglutaconic aciduria type 9 Is a 3-Methylglutaconic aciduria true Inferred relationship Some
3-methylglutaconic aciduria type 9 Is a Developmental hereditary disorder true Inferred relationship Some
3-methylglutaconic aciduria type 9 Is a Severe intellectual disability true Inferred relationship Some
3-methylglutaconic aciduria type 9 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
3-methylglutaconic aciduria type 9 Pathological process Pathological developmental process true Inferred relationship Some 1
3-methylglutaconic aciduria type 9 Interprets Adaptation behaviour true Inferred relationship Some 2
3-methylglutaconic aciduria type 9 Has interpretation Impaired true Inferred relationship Some 2
3-methylglutaconic aciduria type 9 Interprets Intellectual ability true Inferred relationship Some 3
3-methylglutaconic aciduria type 9 Has interpretation Impaired true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start