Synonym(s): - Familial intestinal polyatresia syndrome
Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease Entire classification		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities - See
Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		External references: 1 OMIM reference - See No MeSH references
More Info - Orphanet

Gene symbol	UniProt reference	OMIM reference
TTC7A	Q9ULT0	609332

- Autosomal recessive inheritance
- Duodenal atresia / stenosis / megaduodenum
- Intestinal atresia / stenosis / absence / agenesis / hypoplasia (excludes duodenum)
- Stillbirth / neonatal death

- Polyhydramnios