OBO ID: DOID:2236 |
Term Name: | congenital afibrinogenemia | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I). https://ghr.nlm.nih.gov/condition/congenital-afibrinogenemia#synonyms | ||
References: |
|
||
Ontology: | Human Disease ( DOID:2236 ) |
OTHER congenital afibrinogenemia PAGES
ZEBRAFISH MODELS
Fish | Conditions | Citations |
---|---|---|
fgaug701/ug701 (AB) | standard conditions | Fish et al., 2014 |
fgaug702/ug702 (AB) | standard conditions | Fish et al., 2014 |
fgaug703/ug703 (AB) | standard conditions | Fish et al., 2014 |
PHENOTYPE
No data available
CITATIONS (3)
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.