RS120074118 SMPD1;APBB1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Niemann-Pick disease
type B
Sphingomyelin/cholesterol lipidosis
type A
SMPD1-related disorder
autosomal recessive SMPD1-related disorders
Niemann-Pick disease
type B
Sphingomyelin/cholesterol lipidosis
type A
SMPD1-related disorder
autosomal recessive SMPD1-related disorders