About   Help   FAQ
Disease Ontology Browser
Hermansky-Pudlak syndrome 3 (DOID:0060541)
Alt IDs: OMIM:614072
Definition: A type of Hermasky-Pudlak syndrome caused by homozygous or compound heterozygous mutation in the HPS3 gene on chromosome 3q24.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.08
The Jackson Laboratory