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Dictionary » Dysfibrinogenemia, familial
 

Dysfibrinogenemia, familial

Introduction: Dysfibrinogenemia, familial

Description of Dysfibrinogenemia, familial

Dysfibrinogenemia, familial (medical condition): A rare familial disorder characterized by abnormal fibrinogen. There...more »

See also:

Dysfibrinogenemia, familial:
  »Introduction: Dysfibrinogenemia, familial
  »Symptoms of Dysfibrinogenemia, familial

Dysfibrinogenemia, familial: Related Topics

These medical condition or symptom topics may be relevant to medical information for Dysfibrinogenemia, familial:

Dysfibrinogenemia, familial: Rare Disease

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Dysfibrinogenemia, familial as a "rare disease".

Source - Orphanet

Dysfibrinogenemia, familial as a Disease

Dysfibrinogenemia, familial (medical condition): See Dysfibrinogenemia, familial (disease information).
  »Introduction: Dysfibrinogenemia, familial
  »Symptoms of Dysfibrinogenemia, familial

Dysfibrinogenemia, familial: Related Diseases

Dysfibrinogenemia, familial: Dysfibrinogenemia, familial is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Dysfibrinogenemia, familial:

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