Hypofibrinogenemia

Symptom Information:

Symptom ID: HPO:0011900
Synonyms:
Hypofibrinogenemia [OMIM:Hypofibrinogenemia]
Quality:
Cross references:
OMIM: "Hypofibrinogenemia" [OMIM:Hypofibrinogenemia]
Is a (Direct Parents):
HPO         Abnormality of circulating fibrinogen
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of coagulation(HPO:0001928)
             Abnormality of the coagulation cascade(HPO:0003256)
                Abnormality of the common coagulation pathway(HPO:0010990)
                   Abnormality of circulating fibrinogen(HPO:0011898)
                      Hypofibrinogenemia(HPO:0011900)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
Familial hypofibrinogenemia (Orphanet:101041)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 (OMIM:267700)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3 (OMIM:608898)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4 (OMIM:603552)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
X-linked lymphoproliferative disease (Orphanet:2442)