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
|