loading...| Preferred Name | paroxysmal nocturnal hemoglobinuria | |
| Synonyms |
|
|
| Definitions |
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. NT MGI. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_0060284 |
|
| comment |
NT MGI. |
|
| created by |
emitraka |
|
| creation_date |
2015-02-04T16:30:50Z |
|
| database_cross_reference |
SNOMEDCT_US_2023_03_01:191226006 UMLS_CUI:C0019050 SNOMEDCT_US_2023_03_01:154805009 UMLS_CUI:C0024790 MESH:D006457 SNOMEDCT_US_2023_03_01:1468004 UMLS_CUI:C0086774 ICD10CM:D59.5 ICD10CM:D59.6 GARD:7337 MIM:300818 MIM:615399 NCI:C61233 ORDO:447 |
|
| 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. NT MGI. |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:0060284 |
|
| in_subset | ||
| label |
paroxysmal nocturnal hemoglobinuria |
|
| notation |
DOID:0060284 |
|
| note |
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. NT MGI. |
|
| preferred label |
paroxysmal nocturnal hemoglobinuria |
|
| prefLabel |
paroxysmal nocturnal hemoglobinuria |
|
| subClassOf |