DiseaseID 4180
血友病A
disease
NCI2016_02D:An inherited deficiency of coagulation factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an X-linked recessive disease, hemophilia A is the most c
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Disease: 1Formula: 11Herb: 12Symptom: 12Target: 23Links: 59
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4180
- Core Entity Id
- 60490
- Source Entity Count
- 1
- Preferred Name
- Hemophilia A
- Name Cn
- 血友病A
- Name Pinyin
- Xue You Bing A
- Name En
- Hemophilia A
- 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
- genetic disease
- Hpo Class
- Abnormality of blood and blood-forming tissues
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Abnormality of blood and blood-forming tissues
- Do Class Name
- genetic disease
- Disease Definition
- NCI2016_02D:An inherited deficiency of coagulation factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an X-linked recessive disease, hemophilia A is the most common hemophilia, occurring in approximately 1 in 10,000 male births.|MSH2017_2016_08_12:The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.|CSP2006:classic hemophilia resulting from a deficiency of factor VIII; an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hemophilia A
Role
preferred
Name
Factor Viii Deficiency
Role
preferred
Name
Autosomal Hemophilia A
Role
preferred
Name
Reduced Factor Viii Activity
Role
preferred
Name
HEMA
Role
alias
Name
HEMOPHILIA, CLASSIC
Role
alias
Name
Hereditary Factor Viii Deficiency
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0003125
Herb
HBDIS001316HBDIS021464HBDIS021465HBDIS025086
Me Sh
D006467
Omim
134500306700
Umls
C0019069C3494187
Icd10
D66
Sym Map
SMDE04749SMDE08617
Do Class
DOID:630
Dis Ge Net
C0019069C3494186C3494187C4025649
Umls Sty
T033T047
Hpo Class
HP:0001871
Me Sh Class
C15C16
Etcm Disease
Factor Viii DeficiencyHemophilia a
Tcmbank Disease
114531236613603274373447
Itcmdb Generated
ITX-DISEASE-05993CCC984EITX-DISEASE-568177F1B080ITX-DISEASE-90C95BB910E8
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Page Title
Disease Factor Viii Deficiency Details pageDisease Hemophilia a Details page
Do Class Name
genetic disease
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of blood and blood-forming tissues
Do Disease Class
genetic disease
Hpo Disease Class
Abnormality of blood and blood-forming tissues
Umls Disease Type
Disease or SyndromeFinding
Basic Information
Disease Name
Factor Viii Deficiency
Global Category
Genetic diseases
Anatomical Category
Blood diseases
Disease Name
Hemophilia a
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases;Neuronal diseases
Disease Definition
NCI2016_02D:An inherited deficiency of coagulation factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an X-linked recessive disease, hemophilia A is the most common hemophilia, occurring in approximately 1 in 10,000 male births.|MSH2017_2016_08_12:The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.|CSP2006:classic hemophilia resulting from a deficiency of factor VIII; an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or SyndromeFinding