Afibrinogenemia, congenital

Symptoms of Afibrinogenemia, congenital

Clinical features: Imported from Human Phenotype Ontology (HPO)

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Genetics of Afibrinogenemia, congenital

Modes of inheritance: Autosomal recessive inheritance (HPO, OMIM, Orphanet) ...Source: GTR (NCBI/NIH)1 ...

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Treatments

See also the following treatment articles:

Causes

See also causal information:

Names and Terminology

Synonyms: HYPOFIBRINOGENEMIA, CONGENITAL, SEVERE ...Source: GTR (NCBI/NIH)2 ...

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References

  1. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ CN071205/ 
  2. ibid.

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