Please sign in to follow a disease.

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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary disease (18187) ↑ Omphalocele (3)

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

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.