Human genes for multiple intestinal atresia
Multiple intestinal atresia [DOID:14671]
An intestinal disease characterized by the presence of numerous atresic segments in the small and large intestines that has_material_basis_in homozygous or compound heterozygous mutation in TTC7A on chromosome 2p21.
Synonyms: multiple intestinal atresia, DOID:14671, multiple intestinal atresias, familial intestinal polyatresia syndrome, gastrointestinal defects and immunodeficiency syndrome ...
Linkouts: OMIM