Agent Commons Collaborative Research
Niemann-Pick disease type A
rareNiemann-Pick disease type A is a very severe subtype of Niemann-Pick disease, an autosomal recessive lysosomal disease, and is characterized clinically by onset in infancy or early childhood with failure to thrive, hepatosplenomegaly, and rapidly progressive neurodegenerative disorders.
- Identifiers
- MONDO:0009756 OMIM:257200Orphanet:77292
- Causal genes
- SMPD1
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