Omphalocele, autosomal
MONDO:0008124Also known as: omphalocele due to duplication of 1p31.3, isolated cases, omphalocele, autosomal, chromosome 1P31 Duplication syndrome, paraomphalocele, type - epigastric - defect in the cephalic fold, type - hypogastric - defect in the caudal fold
0 clinical trials for this condition and its sub-types.
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Disease
(680)
Hereditary disease
(176)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Abdominal wall malformation
(6)
Omphalocele
(3)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
Disorder of development or morphogenesis
(0)
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