Genes | GeDiPNet - Gene Disease Pathway & Associations

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All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "F"

131 to 140 of 433 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
131	2232	FDXR	Ferredoxin reductase	ADR, ADXR, ANOA, MMDS9B	Auditory neuropathy, Auditory neuropathy with optic atrophy, Optic atrophy
132	2235	FECH	Ferrochelatase	EPP, EPP1, FCE	Erythropoietic protoporphyria, Bile duct disease, Metabolic syndrome, Migraine, Porphyria
133	2237	FEN1	Flap structure-specific endonuclease 1	FEN-1, MF1, RAD2	Colorectal cancer, Colorectal neoplasm, Crohn disease, Non-immune hydrops fetalis, Inflammatory bowel disease, Lung neoplasms, Ulcerative colitis
134	2241	FER	FER tyrosine kinase	PPP1R74, TYK3, p94-Fer	Asthma, Coronary artery disease, Duane retraction syndrome, Major depressive disorder, Psoriasis, Psychiatric disorders, Respiratory system infectious disease, Schizophrenia, Severe acute respiratory syndrome, Hypertension
135	2242	FES	FES proto-oncogene, tyrosine kinase	FPS	Androgenetic alopecia, Atrial fibrillation, Attention deficit hyperactivity disorder, Cardiovascular disease, Ischemic heart disease, Coronary artery disease, Diabetes mellitus, Hypertension, Insomnia, Myocardial infarction, Myocardial ischemia, Osteoarthritis, Post-traumatic stress disorder, Schizophrenia
136	2243	FGA	Fibrinogen alpha chain	AMYLD2, Fib2	Amyloidosis, Cerebrovascular disorder, Cholelithiasis, Thromboembolic pulmonary hypertension, Congenital afibrinogenemia, Dysfibrinogenemia, Afibrinogenemia, Hypofibrinogenemia, Visceral amyloidosis, Visceral myopathy, Heart disease, Kidney disease, Mouth neoplasm, Osteoporosis, Stroke, Ventricular dysfunction View all (1 more)
137	2244	FGB	Fibrinogen beta chain	HEL-S-78p	Cardiovascular disease, Carotid artery disease, Ischemic heart disease, Obstructive pulmonary disease, Congenital afibrinogenemia, Coronary artery disease, Dysfibrinogenemia, Afibrinogenemia, Hypofibrinogenemia, Kidney failure, Myocardial infarction, Myocardial ischemia, Osteoporosis, Parkinson disease, Stroke, Ventricular fibrillation View all (1 more)
138	2245	FGD1	FYVE, RhoGEF and PH domain containing 1	AAS, FGDY, MRXS16, ZFYVE3	Aarskog-scott syndrome, Attention deficit hyperactivity disorder, Congenital neurologic anomalies�, Craniofacial abnormalities, Desbuquois syndrome, Growth disorder, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Urogenital abnormalities, X-linked intellectual disability
139	2246	FGF1	Fibroblast growth factor 1	AFGF, ECGF, ECGF-beta, ECGFA, ECGFB, FGF-1, FGF-alpha, FGFA, GLIO703, HBGF-1, HBGF1	Brain ischemia, Hypotension, Lethal congenital contracture syndrome, Mesothelioma, Myocardial infarction, Myocardial ischemia, Ovarian neoplasm, Pulmonary fibrosis, Schizophrenia
140	2247	FGF2	Fibroblast growth factor 2	BFGF, FGF-2, FGFB, HBGF-2	Bone disease, Brain infarction, Brain injuries, Cardiomegaly, Skin ulcer, Delirium, dementia, and cognitive disorders, Major depressive disorder, Dermatitis, Gestational diabetes, Diabetic neuropathy, Diabetic retinopathy, Tonic-clonic epilepsy, Erectile dysfunction, Gastric ulcer, Glioma View all (17 more)

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