Taxon:

Human

Gene:

RET or other modifier gene

Chromosome:

10

Location:

10q11.2

Description:

Familial Hirschsprung disease. Affected patients with familial Hirschsprung disease were more likely to inherit the mutant RET protooncogene (10q11.2) from their mothers (Peretz H et al, 1997).

Category:

Parental effect

Record:

62

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