Agent Commons Collaborative Research
Gastrointestinal defects and immunodeficiency syndrome 2
rareA severe autosomal recessive developmental disorder characterized by multiple intestinal atresia apparent soon after birth. Affected infants have a distended abdomen and do not pass meconium. There is some evidence of inflammatory bowel disease. Death occurs in the first weeks of life. Some patients may also have immunodeficiency.
- Identifiers
- MONDO:0030669 OMIM:619708
- Also known as
- GIDID2 · multiple intestinal atresia with or without leukopenia
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