GenTIGSA Gene Database on Rare Genetic Disorders
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3-Methylglutaconic Aciduria Type 2  
Disease Aliases (38)

3 methylglutaconic aciduria, type ii

3 methylglutaconicaciduria type 2

3-methylglutaconic aciduria, type ii

3-methylglutaconic aciduria, type 2

3-methylglutaconicaciduria type 2

3-methylglutaconicaciduria type 2s

3-methylglutaconicaciduria type ii

3-methylglutaconicaciduria type iis

3-methylglutaconic aciduria type 2

3-methylglutaconic aciduria type ii

Barth syndrome; bths

Bths

Barth syndrome

Cardiomyopathy, dilated, x-linked fatal infantile

Cardioskeletal myopathy with neutropenia and abnormal mitochondria

Cardioskeletal myopathy-neutropenia

Cardioskeletal myopathy-neutropenia syndrome

Dilated cardiomyopathy 3a

Endomyocardial fibroelastosis

Left ventricular noncompaction, isolated, x-linked

Left ventricular noncompaction, x-linked

Mga type 2

Mga type 2s

Mga type ii

Mga type iis

Mga, type ii

Mga2

Mgca2

Mga, type 2

Syndrome, barth

Taz defect

Taz-related dilated cardiomyopathy

Type 2, 3-methylglutaconicaciduria

Type 2, mga

Type 2s, mga

Type ii, mga

Type iis, mga

X-linked cardioskeletal myopathy and neutropenia

Associated Genes (1)
 

NCBI-RefSeq:  TAFAZZIN   (Tafazzin, phospholipid-lysophospholipid transacylase)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of 3-Methylglutaconic aciduria type 2 OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations