Prolonged prothrombin time
Symptom Information:
All diseases associated with this symptom:
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
Congenital factor II deficiency | (Orphanet:325) |
Congenital factor V deficiency | (Orphanet:326) |
Congenital factor X deficiency | (Orphanet:328) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Neonatal hemochromatosis | (Orphanet:446) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
PMM2-CDG | (Orphanet:79318) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Reticular dysgenesis | (Orphanet:33355) |