Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4371 to 4380 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4371
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)

4372
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

4373
Coagulation factor VIII associated 2
HAP40
Venous thromboembolism

4374
Coagulation factor VIII associated 3
HAP40
Venous thromboembolism

4375
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

4376
Fatty acid 2-hydroxylase
FAAH, FAH1, FAXDC1, SCS7, SPG35
Spastic paraplegia, Cerebellar atrophy, Dementia, Leprosy, Neurodegeneration with brain iron accumulation, Scoliosis, Spastic ataxia, Hereditary spastic paraplegia, Upper aerodigestive tract neoplasm, Venous thromboembolism

4377
Fatty acid amide hydrolase
FAAH-1, FAAH1, PSAB
Bipolar disorder, Cannabis abuse, Huntington disease, Major depressive disorder, Obesity, Psoriasis, Schizophrenia, Seizures, Substance abuse

4378
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

4379
FA core complex associated protein 100
C17orf70, FANCX
Fanconi anemia, Schizophrenia

4380
FA core complex associated protein 20
C1orf86, FP7162
Coronary artery disease, Dilated cardiomyopathy, Gout, Hypertrophic cardiomyopathy