Hypoalphalipoproteinemia, primary, 2
MONDO:0032766Also known as: ApoA-I and apoC-III deficiency, combined, HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, hypoalphalipoproteinemia, primary, 2, with or without corneal clouding, Apolipoprotein A-I Deficiency, High Density Lipoprotein Deficiency
0 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Broader categories
Disease
(717)
Metabolic disease
(241)
Hereditary disease
(188)
Inborn errors of metabolism
(47)
Human disease
(15)
Disease of genetic or genomic mechanism
(2)
Hypoalphalipoproteinemia
(1)
Apolipoprotein A-I deficiency
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.