DiseaseID 3648
血友病B
disease
NCI2016_02D:An X-linked inherited bleeding disorder caused by deficiency of the coagulation factor IX.|MSH2017_2016_08_12:A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Chri
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 11Target: 19Links: 35
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3648
- Core Entity Id
- 59878
- Source Entity Count
- 1
- Preferred Name
- Hemophilia B
- Name Cn
- 血友病B
- Name Pinyin
- Xue You Bing B
- Name En
- Hemophilia B
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- NCI2016_02D:An X-linked inherited bleeding disorder caused by deficiency of the coagulation factor IX.|MSH2017_2016_08_12:A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008)|CSP2006:deficiency of blood coagulation factor IX inherited as an X-linked disorder; clinical features resemble those in hemophilia A, but patients present with fewer symptoms.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hemophilia B
Role
preferred
Name
CHRISTMAS DISEASE
Role
alias
Name
F9 DEFICIENCY
Role
alias
Name
FACTOR IX DEFICIENCY
Role
alias
Name
HEMB
Role
alias
Name
HEMOPHILIA B LEYDEN
Role
alias
Name
HEMOPHILIA B(M)
Role
alias
Name
Hereditary Factor Ix Deficiency
Role
alias
Name
PLASMA THROMBOPLASTIN COMPONENT DEFICIENCY
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS000574
Me Sh
D002836
Omim
306900
Umls
C0008533
Icd10
D67
Sym Map
SMDE02379
Do Class
DOID:630DOID:7
Dis Ge Net
C0008533
Umls Sty
T047
Me Sh Class
C15C16
Etcm Disease
Hemophilia B
Tcmbank Disease
15502
Itcmdb Generated
ITX-DISEASE-0D6C48C534FA
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Hemophilia B Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Hemophilia B
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases;Neuronal diseases
Disease Definition
NCI2016_02D:An X-linked inherited bleeding disorder caused by deficiency of the coagulation factor IX.|MSH2017_2016_08_12:A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008)|CSP2006:deficiency of blood coagulation factor IX inherited as an X-linked disorder; clinical features resemble those in hemophilia A, but patients present with fewer symptoms.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome