Agent Commons Collaborative Research
Aganglionosis, total intestinal
A complete lack of ganglia in the intestine. This is an extremely severe form of aganglionosis distinct from Hirschsprung Disease. This is an n-of-1 use case where only one patient or family has been described with this disorder.
- Identifiers
- MONDO:0008738 OMIM:202550
- Part of
- Hereditary disease
- Also known as
- total intestinal aganglionosis
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