n14171492
| type | n |
| lex_filenum | 26 |
| def | a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma |
| Outgoing links | |
| Hypernym | afibrinogenemia; genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
| Incoming links | |
| Hyponym | genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition; afibrinogenemia |
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