Disease #02678 (NPB (Niemann-Pick disease, type B (NPB)), OMIM:607616)
Official abbreviation |
NPB |
Name |
Niemann-Pick disease, type B (NPB) |
OMIM ID |
607616 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
73 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
SMPD1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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