Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4351 to 4360 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4351
Coagulation factor V
FVL, PCCF, RPRGL1, THPH2
Angioedema, Osteonecrosis of the femoral head, Atrial fibrillation, Avascular necrosis of bone, Blood coagulation disorder, Brain ischemia, Budd-chiari syndrome, Cardiovascular disease, Ischemic stroke, Cerebral sinovenous thrombosis, Cerebrovascular disorder, Venous hypertension, Venous insufficiency, Colonic neoplasms, Congenital factor v deficiency
View all (28 more)

4352
Coagulation factor VII
SPCA
Cerebral hemorrhage, Ischemic stroke, Ischemic heart disease, Congenital factor vii deficiency, Coronary artery disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Disseminated intravascular coagulation, Factor vii deficiency, Hematoma, Hematuria, Hemorrhage, Hemorrhagic disease, Hypertension, Intracranial hemorrhage
View all (9 more)

4353
Coagulation factor VIII
AHF, DXS1253E, F8B, F8C, FVIII, HEMA, THPH13
Ankylosing spondylitis, Anti-neutrophil antibody associated vasculitis, Autoimmune disease, Hemophilia a carriers, Factor viii deficiency, Hemophilia a, Thrombophilia, Venous thromboembolism, Venous thrombosis

4354
Coagulation factor VIII associated 2
HAP40
Venous thromboembolism

4355
Coagulation factor VIII associated 3
HAP40
Venous thromboembolism

4356
Coagulation factor IX
F9 p22, FIX, HEMB, P19, PTC, THPH8
Bipolar disorder, Hemophilia b carriers, Hemophilia a, Hemophilia b, Mesothelioma, Neurotic disorder, Thrombophilia, Thrombosis, Venous thromboembolism, Warfarin sensitivity

4357
Fatty acid 2-hydroxylase
FAAH, FAH1, FAXDC1, SCS7, SPG35
Spastic paraplegia, Cerebellar atrophy, Dementia, Neurodegeneration with brain iron accumulation, Scoliosis, Spastic ataxia, Hereditary spastic paraplegia, Upper aerodigestive tract neoplasm, Venous thromboembolism

4358
Fatty acid amide hydrolase
FAAH-1, FAAH1, PSAB
Bipolar disorder, Cannabis abuse, Huntington disease, Major depressive disorder, Obesity, Psoriasis, Schizophrenia, Seizures, Substance abuse

4359
Fatty acid amide hydrolase 2
AMDD
Androgenetic alopecia, Renal cell carcinoma, Hypogonadism, Irritable bowel syndrome, Neurotic disorder, Diabetes mellitus type 2, X-linked complex neurodevelopmental disorder

4360
FA core complex associated protein 100
C17orf70, FANCX
Fanconi anemia, Schizophrenia