About   Help   FAQ
Disease Ontology Browser
paroxysmal nocturnal hemoglobinuria (DOID:0060284)
Alliance: disease page
Alt IDs: OMIM:300818, OMIM:615399, ICD10CM:D59.5, ICD10CM:D59.6, MESH:D006457, NCI:C61233, ORDO:447, UMLS_CUI:C0019050, UMLS_CUI:C0024790, UMLS_CUI:C0086774
Definition: An acquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory