Any congenital diarrhea in which the cause of the disease is a mutation in the GUCY2C gene.
Comprehensive, easy-to-understand information about this condition
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Hirschsprung disease-hearing loss-polydactyly syndrome
MONDO:0009342
Hirschsprung disease-nail hypoplasia-dysmorphism syndrome
MONDO:0009344
oculogastrointestinal muscular dystrophy
MONDO:0010181
Goldberg-Shprintzen syndrome
MONDO:0012280
congenital malabsorptive diarrhea 4
MONDO:0012479
Hirschsprung disease-ganglioneuroblastoma syndrome
MONDO:0013082