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Metadata
ID DOID:0070112
Name Niemann-Pick disease type B
Definition A Niemann-Pick disease characterized by visceral involvement only and survival into adulthood that has_material_basis_in an autosomal recessive mutation of the SMPD1 gene on chromosome 11p15.4.
https://www.ncbi.nlm.nih.gov/pubmed/13696518, https://www.ncbi.nlm.nih.gov/pubmed/12369017
Xrefs

GARD:10729

ICD10CM:E75.2

MIM:607616

Subsets

DO_rare_slim

Parent Relationships

is_a Niemann-Pick disease

Subclass Logical Relationships

disease has basis in some structural_variant

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