3billion
back to listBack to List

SDHA

succinate dehydrogenase complex flavoprotein subunit A

HCNC Approved Symbol
SDHA (HGNC:10680)
Genomic Coordinates
5:218,320 - 268,746 (5p15.33)
Synonyms
FP, SDHF, SDH2
Disease Associations
This gene is associated with the following 4 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Cardiomyopathy, dilated, 1GG
613642AR
Mitochondrial complex II deficiency, nuclear type 1
252011AR
Neurodegeneration with ataxia and late-onset optic atrophy
619259AD
Pheochromocytoma/paraganglioma syndrome 5
614165AD

Diagnosed Cases

4Patients

In total, 4 patients were diagnosed with a variant in the SDHA gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Cardiogenic shock
 2 (50.0%)
Dilated cardiomyopathy
 2 (50.0%)
Hypothyroidism
 2 (50.0%)
Noncompaction cardiomyopathy
 2 (50.0%)
Attention-deficit hyperactivity disorder
 1 (25.0%)