has material basis in germline mutation in NEUROG3 congenital diarrhea congenital malabsorptive diarrhea 4 https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/diarrhea_4_malabsorptive_congenital MONDO:0012479 congenital malabsorptive diarrhea type 4 OMIM:610370 congenital diarrhoea caused by mutation in NEUROG3 congenital malabsorptive diarrhoea type 4 icd11.foundation:302560695 MESH:C563673 diarrhoea 4, malabsorptive, congenital GARD:0016729 NEUROG3 congenital diarrhea DIAR4 SCTID:722392003 NEUROG3 congenital diarrhoea diarrhea 4, malabsorptive, congenital congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells MEDGEN:372151 congenital diarrhea caused by mutation in NEUROG3 congenital malabsorptive diarrhea due to paucity of enteroendocrine cells UMLS:C1835888 Orphanet:83620 enteric anendocrinosis DOID:0060779 Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells is an exceedingly rare genetic gastroenterological disease characterized by severe malabsorptive diarrhea and a lack of intestinal enteroendocrine cells. Within the first weeks of life, patients present with vomiting, dehydration, and severe diarrhea unresponsive to various nutrients and formulas, and require home parenteral nutrition. Diabetes mellitus has also been reported.