has material basis in germline mutation in ERBB3 neuronal intestinal dysplasia chronic intestinal pseudoobstruction visceral neuropathy, familial visceral neuropathy, familial, 1, autosomal recessive https://www.malacards.org/card/neuronal_intestinal_dysplasia_type_a https://www.malacards.org/card/visceral_neuropathy_familial_1_autosomal_recessive visceral neuropathy, familial, autosomal recessive MEDGEN:340946 UMLS:C1855733 Argyrophil myenteric plexus deficiency of NID A DOID:0080679 A form of chronic intestinal pseudoobstruction caused by a developmental failure of the enteric neurons to differentiate or migrate properly and manifests as a bowel obstruction. Orphanet:99811 pseudoobstruction, chronic idiopathic intestinal, neuronal type neuronal intestinal dysplasia, type a Argyrophil myenteric plexus, deficiency of GARD:0003928 OMIM:243180 visceral neuropathy familial MESH:C537394 intestinal pseudoobstruction due to neuronal disease MONDO:8000011 pseudoobstruction chronic idiopathic intestinal neuronal type