Abnormality of coagulation
Symptom Information:
Symptom ID: | HPO:0001928 | |||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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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) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477) Abnormality of coagulation(HPO:0001928) Abnormal bleeding(HPO:0001892) Abnormality of coagulation(HPO:0001928) Vascular disorders(MedDRA:10047065) Vascular haemorrhagic disorders(MedDRA:10047075) Haemorrhages NEC(MedDRA:10018987) Abnormal bleeding(HPO:0001892) Abnormality of coagulation(HPO:0001928) Abnormality of coagulation(HPO:0001928) Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) Coagulation and bleeding analyses(MedDRA:10009728) Abnormal bleeding(HPO:0001892) Abnormality of coagulation(HPO:0001928) |
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Database Frequency: | 44 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALG2-CDG | (Orphanet:79326) |
Argininemia | (Orphanet:90) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
B4GALT1-CDG | (Orphanet:79332) |
BLEEDING DISORDER, PLATELET-TYPE, 14 | (OMIM:614158) |
Blue rubber bleb nevus | (Orphanet:1059) |
Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
Congenital disorder of glycosylation | (Orphanet:137) |
DK1-CDG | (Orphanet:91131) |
Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
Dubin-Johnson syndrome | (Orphanet:234) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Fetal Gaucher disease | (Orphanet:85212) |
Fetal cytomegalovirus syndrome | (Orphanet:294) |
GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN | (OMIM:137900) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
INTEGRIN, BETA-3 | (OMIM:173470) |
Indomethacin embryofetopathy | (Orphanet:1909) |
Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
MEGDEL syndrome | (Orphanet:352328) |
Malignant peritoneal mesothelioma | (Orphanet:168811) |
Mediterranean macrothrombocytopenia | (Orphanet:101022) |
Multiple sclerosis - ichthyosis - factor VIII deficiency | (Orphanet:3151) |
Neonatal hemochromatosis | (Orphanet:446) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
SLC35A2-CDG | (Orphanet:356961) |
SRD5A3-CDG | (Orphanet:324737) |
Sitosterolemia | (Orphanet:2882) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Transaldolase deficiency | (Orphanet:101028) |
Tyrosinemia type 1 | (Orphanet:882) |
Von Willebrand disease | (Orphanet:903) |
Wilson disease | (Orphanet:905) |
Wolfram syndrome 2 | (OMIM:604928) |
Zellweger syndrome | (Orphanet:912) |