congenital malabsorptive diarrhea 4
congenital diarrhea characterized by chronic unremitting malabsorptive diarrhea and a profound dysgenesis of the enteroendocrine cells that has material basis in mutation in the gene encoding neurogenin-3 (NEUROG3) on chromosome 10q21.3
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congenital malabsorptive diarrhea 4
Summary
congenital malabsorptive diarrhea 4 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- congenital malabsorptive diarrhea 4's instance of is recorded as rare disease[3].
- congenital malabsorptive diarrhea 4's instance of is recorded as class of disease[4].
- congenital malabsorptive diarrhea 4 is a type of congenital diarrhea[5].
- congenital malabsorptive diarrhea 4 is a type of congenital enteropathy involving intestinal mucosa development[6].
- congenital malabsorptive diarrhea 4 is a type of genetic disease[7].
- congenital malabsorptive diarrhea 4's genetic association is recorded as NEUROG3[8].
- congenital malabsorptive diarrhea 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060779[9].
- congenital malabsorptive diarrhea 4's exact match is recorded as http://identifiers.org/doid/DOID:0060779[10].
- congenital malabsorptive diarrhea 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
congenital malabsorptive diarrhea 4 is known by 7 alternative names across languages and contexts.[2]