| Descriptor English: | Afibrinogenemia | ||||||
| Descriptor Spanish: |
Afibrinogenemia
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| Descriptor Portuguese: | Afibrinogenemia | ||||||
| Descriptor French: | Afibrinogénémie | ||||||
| Entry term(s): |
Afibrinogenaemia, Congenital Afibrinogenaemias, Congenital Afibrinogenemia, Congenital Afibrinogenemia, Familial Afibrinogenemias Afibrinogenemias, Congenital Afibrinogenemias, Familial Congenital Afibrinogenaemia Congenital Afibrinogenaemias Congenital Afibrinogenemia Congenital Afibrinogenemias Congenital Hypofibrinogenemia Congenital Hypofibrinogenemias Deficiency, Fibrinogen Familial Afibrinogenemia Familial Afibrinogenemias Fibrinogen Deficiencies Fibrinogen Deficiency Hypofibrinogenemia, Congenital Hypofibrinogenemias, Congenital |
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| Tree number(s): |
C15.378.100.100.056 C15.378.100.141.072 C15.378.463.067 C16.320.099.056 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000347 | ||||||
| Scope note: | A deficiency or absence of FIBRINOGEN in the blood. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital 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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| DeCS ID: | 352 | ||||||
| Unique ID: | D000347 | ||||||
| NLM Classification: | WH 322 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1966/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2018/06/13 |
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Afibrinogenemia
- Preferred
Congenital Afibrinogenemia
- Related but not broader or narrower
Deficiency, Fibrinogen
- Narrower
| Concept UI |
M0000532 |
| Scope note | A deficiency or absence of FIBRINOGEN in the blood. |
| Preferred term | Afibrinogenemia |
| Entry term(s) |
Afibrinogenemias |
| Concept UI |
M0583452 |
| Preferred term | Congenital Afibrinogenemia |
| Entry term(s) |
Afibrinogenaemia, Congenital Afibrinogenaemias, Congenital Afibrinogenemia, Congenital Afibrinogenemia, Familial Afibrinogenemias, Congenital Afibrinogenemias, Familial Congenital Afibrinogenaemia Congenital Afibrinogenaemias Congenital Afibrinogenemias Congenital Hypofibrinogenemia Congenital Hypofibrinogenemias Familial Afibrinogenemia Familial Afibrinogenemias Hypofibrinogenemia, Congenital Hypofibrinogenemias, Congenital |
| Concept UI |
M000636808 |
| Preferred term | Deficiency, Fibrinogen |
| Entry term(s) |
Fibrinogen Deficiencies Fibrinogen Deficiency |
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