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About:
3-Methylglutaconic aciduria type 2
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New Facet based on Instances of this Class
Attributes
Values
label
3-methylglutaconic aciduria type 2
COEXISTS_WITH
Neutropenia
ASSOCIATED_WITH
Mutation
schema:identifier
c0574083
ISA
Disease
Hereditary Diseases
Metabolic Diseases
Neuromuscular Diseases
Multisystem disorder
CAUSES
Heart failure
Functional disorder
Cardiomyopathies
PROCESS_OF
C0030705
Family
Human
Child
Individual
Mus
Participant
cohort
Brothers
Infant, Newborn
Boys
Young adult
Adolescent
Youth
Toddler
AFFECTS
Individual
Boys
Muscular Dystrophy, Duchenne
OCCURS_IN
Boys
MANIFESTATION_OF
Disease
is
LOCATION_OF
of
Heart
is
COEXISTS_WITH
of
Myopathy
Cardiomyopathies
Cardiomyopathy, Dilated
Neutropenia
Death, Sudden
CARDIAC PROBLEM
Short stature
Growth delay
Dilated cardiomyopathy secondary to metabolic disorder
is
ASSOCIATED_WITH
of
Genes
Metabolism
Orthologous Gene
Cardiolipins
metabolomics
Transcriptional Coactivator with PDZ-Binding Motif|TAZ
Germinal mosaicism
is
CAUSES
of
Genes
genetic locus
Mutation
Transcriptional Coactivator with PDZ-Binding Motif|TAZ
is
TREATS
of
Therapeutic procedure
agonists
Screening Tests
resistance education
Diagnostic Services
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