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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Visceral neuropathy, familial
Visceral neuropathy, familial, 3, autosomal dominant
rare
Identifiers
MONDO:0012317
OMIM:609629
Part of
Chronic intestinal pseudoobstruction
Visceral neuropathy, familial
Also known as
visceral neuropathy, familial, autosomal dominant
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