Fanconi anemia
MONDO:0019391Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.
Also known as: Fanconi anemia, Fanconi pancytopenia, Fanconi's anemia, Panmyelopathy, Fanconi, pancytopenia, congenital, primary erythroid hypoplasia
49 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Fanconi anemia complementation group A
(4)
Fanconi anemia complementation group D1
(4)
Fanconi anemia complementation group E
(4)
Fanconi anemia, complementation group S
(2)
Fanconi anemia complementation group N
(1)
Fanconi anemia, complementation group 10
(0)
Fanconi anemia complementation group B
(0)
Fanconi anemia complementation group C
(0)
Fanconi anemia complementation group D2
(0)
Fanconi anemia complementation group F
(0)
Fanconi anemia complementation group G
(0)
Fanconi anemia complementation group I
(0)
Fanconi anemia complementation group J
(0)
Fanconi anemia complementation group L
(0)
Fanconi anemia complementation group O
(0)
Fanconi anemia complementation group P
(0)
Fanconi anemia complementation group Q
(0)
Fanconi anemia complementation group R
(0)
Fanconi anemia complementation group T
(0)
Fanconi anemia complementation group U
(0)