Gastrointestinal defect and immunodeficiency syndrome
MONDO:0030831A rare hereditary disease characterized by intestinal obstruction and profound combined immune deficiency.
Also known as: hereditary multiple intestinal atresia
6 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
Disease
(618)
Hereditary disease
(172)
Digestive system disorder
(141)
Intestinal disorder
(55)
Human disease
(14)
Intestinal atresia
(3)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)