| Descriptor English: | Hemophilia A | ||||||
| Descriptor Spanish: |
Hemofilia A
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| Descriptor Portuguese: | Hemofilia A | ||||||
| Descriptor French: | Hémophilie A | ||||||
| Entry term(s): |
As, Autosomal Hemophilia Autosomal Hemophilia A Autosomal Hemophilia As Classic Hemophilia Classic Hemophilias Congenital Hemophilia A Congenital Hemophilia As Deficiency, Factor VIII Factor 8 Deficiency, Congenital Factor VIII Deficiency Factor VIII Deficiency, Congenital Haemophilia Hemophilia Hemophilia A, Autosomal Hemophilia A, Congenital Hemophilia As Hemophilia As, Autosomal Hemophilia As, Congenital Hemophilia, Classic Hemophilias, Classic |
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| Tree number(s): |
C15.378.100.100.500 C15.378.100.141.500 C15.378.463.500 C16.320.099.500 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006467 | ||||||
| Scope note: | 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 99; see HEMOPHILIA 1966-98; for HEMOPHILIA A see HEMOPHILIA 1993-98 |
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| History Note: | 99(66) |
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| Related: |
Factor VIII
MeSH Hemarthrosis MeSH Hemophilia B MeSH | ||||||
| DeCS ID: | 6619 | ||||||
| Unique ID: | D006467 | ||||||
| NLM Classification: | WH 325 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1999/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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Hemophilia A
- Preferred
Autosomal Hemophilia A
- Narrower
Factor VIII Deficiency
- Related but not broader or narrower
| Concept UI |
M0010149 |
| Scope note | 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. |
| Preferred term | Hemophilia A |
| Entry term(s) |
Classic Hemophilia Classic Hemophilias Congenital Hemophilia A Congenital Hemophilia As Haemophilia Hemophilia Hemophilia A, Congenital Hemophilia As Hemophilia As, Congenital Hemophilia, Classic Hemophilias, Classic |
| Concept UI |
M0574711 |
| Preferred term | Autosomal Hemophilia A |
| Entry term(s) |
As, Autosomal Hemophilia Autosomal Hemophilia As Hemophilia A, Autosomal Hemophilia As, Autosomal |
| Concept UI |
M0574712 |
| Preferred term | Factor VIII Deficiency |
| Entry term(s) |
Deficiency, Factor VIII Factor 8 Deficiency, Congenital Factor VIII Deficiency, Congenital |
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