RS1360462093 VPS33B
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Associated Conditions
Keratoderma-ichthyosis-deafness syndrome
autosomal recessive
Arthrogryposis
renal dysfunction
and cholestasis 1
Cholestasis
progressive familial intrahepatic
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Keratoderma-ichthyosis-deafness syndrome
autosomal recessive
Arthrogryposis
renal dysfunction
and cholestasis 1
Cholestasis
progressive familial intrahepatic
Other Variants in VPS33B