PedAM
Pediatric Disease Annotations & Medicines
| factor xiii deficiency | ||||
| Disease ID | 936 |
|---|---|
| Disease | factor xiii deficiency |
| Definition | A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis. |
| Synonym | defic factor xiii deficiencies, factor xiii deficiency of factor xiii deficiency, factor xiii deficiency, laki-lorand factor factor xiii defic factor xiii deficiencies factor xiii deficiency [disease/finding] factor xiii deficiency disease factor xiii deficiency disease (disorder) factor xiii deficiency disease, nos factor xiii deficiency, congenital fibrin stabilising factor deficiency fibrin stabilizing factor deficiency fibrin stabilizing factor deficiency, congenital fibrinase deficiency, congenital hereditary factor xiii deficiency hereditary factor xiii deficiency disease hereditary factor xiii deficiency disease (disorder) hereditary fibrin stabilizing factor deficiency laki-lorand factor deficiency disease laki-lorand factor deficiency, congenital |
| DOID | |
| UMLS | C0015530 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:6) C0085273 | parvovirus b19 infection | 2 C0021359 | infertility | 1 C0034152 | henoch-schonlein purpura | 1 C0003873 | rheumatoid arthritis | 1 C0040034 | thrombocytopenia | 1 C0003486 | aortic aneurysm | 1 |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:2) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:30) 1361 | CPB2 | DISEASES 3053 | SERPIND1 | DISEASES 2158 | F9 | DISEASES 5327 | PLAT | DISEASES 2765 | GML | DISEASES 5054 | SERPINE1 | DISEASES 7035 | TFPI | DISEASES 55640 | FLVCR2 | DISEASES 10343 | PKDREJ | DISEASES 7450 | VWF | DISEASES 2162 | F13A1 | DISEASES 3700 | ITIH4 | DISEASES 83706 | FERMT3 | DISEASES 5473 | PPBP | DISEASES 3673 | ITGA2 | DISEASES 10855 | HPSE | DISEASES 948 | CD36 | DISEASES 2147 | F2 | DISEASES 5340 | PLG | DISEASES 5345 | SERPINF2 | DISEASES 2 | A2M | DISEASES 2152 | F3 | DISEASES 2335 | FN1 | DISEASES 23038 | WDTC1 | DISEASES 2165 | F13B | DISEASES 462 | SERPINC1 | DISEASES 2153 | F5 | DISEASES 2155 | F7 | DISEASES 2877 | GPX2 | DISEASES 2160 | F11 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 936 |
|---|---|
| Disease | factor xiii deficiency |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:7) HP:0012223 | Ruptured spleen | 2 HP:0001370 | Rheumatoid arthritis | 1 HP:0001873 | Low platelet count | 1 HP:0000789 | Infertility | 1 HP:0001892 | Bleeding diathesis | 1 HP:0100309 | Subdural hemorrhage | 1 HP:0004942 | Aortic aneurysm | 1 |
| Disease ID | 936 |
|---|---|
| Disease | factor xiii deficiency |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:2) |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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| (Waiting for update.) |
Chemical(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
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| (Waiting for update.) | |