Hereditary anemia
MONDO:0016624Also known as: constitutional deficiency anemia, constitutional rare deficiency anaemia, constitutional rare deficiency anemia, inherited deficiency anemia
51 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Thiamine-responsive megaloblastic anemia syndrome
(5)
Methylmalonic aciduria and homocystinuria type cblC
(3)
Methylcobalamin deficiency type cblE
(2)
Methylcobalamin deficiency type cblG
(2)
Methylmalonic aciduria and homocystinuria type cblD
(2)
Hereditary intrinsic factor deficiency
(1)
Methylmalonic acidemia with homocystinuria, type cblJ
(1)
Methylmalonic aciduria and homocystinuria
(1)
Methylmalonic aciduria and homocystinuria type cblF
(1)
Orotic aciduria
(1)
Transcobalamin II deficiency
(1)
Aceruloplasminemia
(0)
Atransferrinemia
(0)
Constitutional megaloblastic anemia with severe neurologic disease
(0)
Formiminoglutamic aciduria
(0)
Hereditary folate malabsorption
(0)
Homocystinuria-megaloblastic anemia cblD type
(0)
Homocystinuria without methylmalonic aciduria
(0)
Imerslund-Grasbeck syndrome
(0)
Imerslund-Grasbeck syndrome type 1
(0)