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 |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-12-24 09:21:26 +01:00 (CET) |
Individuals
|