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Multiple acyl-CoA dehydrogenation deficiency, mild type
3 associated genes
28 connected diseases
No signs/symptoms info
Disease Type of connection
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type
Familial isolated dilated cardiomyopathy
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Early-onset autosomal dominant Alzheimer disease
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Autosomal dominant hypohidrotic ectodermal dysplasia
Behavioral variant of frontotemporal dementia
Estrogen resistance syndrome
Familial renal cell carcinoma
Huntington disease
Juvenile Huntington disease
Left ventricular noncompaction
Muscular dystrophy, Selcen type
Progressive non-fluent aphasia
Semantic dementia
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Acute fatty liver of pregnancy
Leigh syndrome with nephrotic syndrome
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Mitochondrial trifunctional protein deficiency
Pyruvate dehydrogenase E3 deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
ETFA P13804608053
ETFB P38117130410
ETFDH Q16134231675
No signs/symptoms info available.