Hypofibrinogenemia
Symptom Information:
Symptom ID: | HPO:0011900 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |