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Summary
SIALURIA
SIALURIA, FRENCH TYPE
269921
OMIM = Online Medalian Inheritance of Men
3166
9p13.3
very rare
autosomal dominant

symptoms
apnea
developmental delay
dysmorphism
hepatomegaly (large liver)
inguinal hernia
onset, childhood
scoliosis
seizures
splenomegaly (large spleen)
syndactyly
laboratory finding
Literature