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loading...| Preferred Name |
Hemophilia |
| ID |
http://www.orpha.net/ORDO/Orphanet_448 |
| definition |
A rare hematological disorder characterized by spontaneous hemorrhage or prolonged bleeding due to factor VIII or IX deficiency. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=448 |
| has_age_of_onset |
Antenatal Neonatal Infancy |
| has_inheritance |
X-linked recessive |
| hasDbXref |
MedDRA:10061992 UMLS:C0684275 |
| label |
Hemophilia |
| notation |
Clinical group ORPHA:448 |
| prefixIRI |
ORDO:Orphanet_448 |
| prefLabel |
Hemophilia |
| present_in |
China AND has_point_prevalence_average_value : 6.46 AND has_point_prevalence_range : 1-9 / 100 000 Europe AND has_point_prevalence_average_value : 7.7 AND has_point_prevalence_range : 1-9 / 100 000 Europe AND has_annual_incidence_average_value : 6.25 AND has_annual_incidence_range : 1-9 / 100 000 |
| subClassOf |
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