Omphalocele, autosomal

MONDO:0008124

Also 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, 0 tagged with Omphalocele, autosomal itself.

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↑ Hereditary disease (18187) ↑ Omphalocele (3)

Including sub-types (0) Tagged with Omphalocele, autosomal (0)

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