Abnormality of the coagulation cascade
Symptom Information:
| Symptom ID: | HPO:0003256 | ||||
| Synonyms: |
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| 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) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477) Abnormality of the coagulation cascade(HPO:0003256) |
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| Database Frequency: | 19 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
| Acute infantile liver failure-multisystemic involvement syndrome | (Orphanet:370088) |
| Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
| Congenital bile acid synthesis defect type 2 | (Orphanet:79303) |
| Congenital bile acid synthesis defect type 3 | (Orphanet:79302) |
| Congenital bile acid synthesis defect type 4 | (Orphanet:79095) |
| GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN | (OMIM:137900) |
| HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT | (OMIM:300049) |
| HYPERVITAMINOSIS A, SUSCEPTIBILITY TO | (OMIM:240150) |
| Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
| Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
| Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
| King-Denborough syndrome | (Orphanet:99741) |
| MEGDEL syndrome | (Orphanet:352328) |
| Malignant hyperthermia | (Orphanet:423) |
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
| Nodular neuronal heterotopia | (Orphanet:2149) |
| PGM1-CDG | (Orphanet:319646) |
| RFT1-CDG | (Orphanet:244310) |