Afibrinogenemia

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Afibrinogenemia" [OMIM:Afibrinogenemia]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Congenital fibrinogen deficiency (Orphanet:335)
Familial afibrinogenemia (Orphanet:98880)
Familial dysfibrinogenemia (Orphanet:98881)
Familial hypodysfibrinogenemia (Orphanet:248408)
Familial hypofibrinogenemia (Orphanet:101041)