Search Ontology:
Human Disease
Niemann-Pick disease type C2
- Term ID
- DOID:0070114
- Synonyms
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- NPC2
- 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
- References
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- GARD:3992
- ICD10CM:E75.2
- MIM:607625
- Ontology
- Human Disease ( DOID:0070114 )
- is a type of
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Genes Involved
Zebrafish Models