Infantile neurovisceral acid sphingomyelinase deficiency

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Name:
Infantile neurovisceral acid sphingomyelinase deficiency
Description:
A rare, autosomal recessive, acid sphingomyelinase deficiency characterized clinically by onset in infancy or early childhood with failure to thrive, hepatosplenomegaly, interstitial lung disease and rapidly progressive neurodegenerative disorders.
ORPHAcode:
77292
Synonyms:
Infantile neurovisceral ASMD
NPD-A
Niemann-Pick disease type A
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14