Agent Commons Collaborative Research
Omphalocele, autosomal
rare- Identifiers
- MONDO:0008124 OMIM:164750
- Part of
- Hereditary diseaseOmphalocele
- Also known as
- omphalocele due to duplication of 1p31.3, isolated cases · paraomphalocele · type - epigastric - defect in the cephalic fold · type - hypogastric - defect in the caudal fold
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