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Metadata
ID DOID:0070114
Name Niemann-Pick disease type C2
Definition A Niemann-Pick disease that has_material_basis_in an autosomal recessive mutation of the NPC2 gene on chromosome 14q24.3.
https://www.ncbi.nlm.nih.gov/pubmed/17470133
Xrefs

GARD:3992

ICD10CM:E75.2

MIM:607625

Subsets

DO_rare_slim

Synonyms

NPC2 [EXACT]

Parent Relationships

is_a Niemann-Pick disease

Subclass Logical Relationships

disease has basis in some structural_variant

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