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. 2021 May 14;8:659550. doi: 10.3389/fmolb.2021.659550

TABLE 2.

Human diseases linked to ALDH genes.

Gene Disease
Aldh1a1 Cataract formation; Parkinson’s disease
Aldh1a2 Disrupted embryonic development; spina bifida; rare cases of congenital heart disease
Aldh1a3 Disrupted embryonic development
Aldh1b1 Hypertension; ethanol sensitivity; ethylmalonic encephalopathy; bipolar disorder
Aldh2 Alcohol intolerance; heart attack; hypertension; cancers; liver cirrhosis; Parkinson’s and late onset Alzheimer’s disease
Aldh3a1 Cataract formation
Aldh3a2 Sjogren-Larsson syndrome
Aldh4a1 Type II hyperprolinemia
Aldh5a1 γ-hydroxybutyric aciduria
Aldh6a1 Psychomotor delay; methylmalonic aciduria
Aldh7a1 Pyridoxine-dependent epilepsy; osteoporosis
Aldh16a1 Gout
Aldh18a1 Hyperammonemia