331
|
|
|
FGFR1 oncogene partner 2 |
HSPC123-like, WIT3.0 |
|
332
|
|
|
Fibroblast growth factor receptor 2 |
BBDS, BEK, BFR-1, CD332, CEK3, CFD1, ECT1, JWS, K-SAM, KGFR, TK14, TK25 |
Ankylosis, Antley-bixler syndrome, Apert syndrome, Atrial fibrillation, Attention deficit hyperactivity disorder, Congenital aural atresia, Benign prostatic hyperplasia, Bent bone dysplasia, Biliary tract cancer, Biliary tract neoplasms, Bipolar disorder, Breast cancer, Breast neoplasms, Byzanthine arch palate, Cancer, Adenoid cystic carcinoma, Cervical cancer, Cholangiocarcinoma, Cleft lip, Cleft palate, Colorectal cancer, Complete unilateral cleft lip, Congenital skin anomaly, Craniofacial abnormalities, Craniofacial dysostosis, Craniosynostosis, Crouzon syndrome, Cutaneous lupus erythematosus, Beare-stevenson cutis gyrata syndrome, Cutis gyrata syndrome, Major depressive disorder, Dermatologic disorder, Desbuquois syndrome, Developmental coordination disorder, Dupuytren contracture, Ectrodactyly, Endometrial cancer, Endometrial neoplasms, Esophageal cancer, Esophageal neoplasms, Estrogen-receptor negative breast cancer, Gastric cancer, Gout, Hepatocellular carcinoma, Hydrocephalus, Intellectual developmental disorder, Lacrimoauriculodentodigital syndrome, Ladd syndrome, Congenital anomaly of limb, Liver cirrhosis, Lung cancer, Lung neoplasms, Auricle malformation, Meier-gorlin syndrome, Motor skills disorder, Non-hodgkins lymphoma, Non-organic psychosis, Ovarian cancer, Ovarian serous carcinoma, Pancreatic cancer, Pelvic organ prolapse, Pfeiffer syndrome, Prostate cancer, Psychotic disorders, Saethre-chotzen syndrome, Schizophrenia, Nonsyndromic hearing loss, Skin abnormalities, Skin disease, Squamous cell carcinoma, Stomach neoplasms, Tooth abnormalities, Triple negative breast cancerView all (58 more) |
333
|
|
|
Fibroblast growth factor receptor 3 |
ACH, CD333, CEK2, HSFGFR3EX, JTK4 |
Achondroplasia, Alzheimer disease, Androgenetic alopecia, Atrial fibrillation, Bladder cancer, Brachycephaly, Camptodactyly, tall stature, and hearing loss syndrome, Transitional cell carcinoma, Cataract, Catshl syndrome, Cervical cancer, Obstructive pulmonary disease, Cleft lip, Cleft palate, Colorectal cancer, Colorectal neoplasms, Complete unilateral cleft lip, Congenital neurologic anomalies, Connective tissue disease, Coronal craniosynostosis, Craniofacial dysostosis, Craniosynostosis, Crouzon syndrome with acanthosis nigricans, Desbuquois syndrome, Diabetes mellitus, Epidermal nevus, Giant cell glioblastoma, Gliosarcoma, Lacrimoauriculodentodigital syndrome, Ladd syndrome, Larsen syndrome, Urinary bladder cancer, Muenke syndrome, Multiple myeloma, Osteoarthritis, Pituitary stalk interruption syndrome, Saethre-chotzen syndrome, Seminoma, Skeletal dysplasia, Testicular germ cell tumor, Thanatophoric dysplasia, Diabetes mellitus type 1, Diabetes mellitus type 2, Urinary bladder neoplasms, Uterine neoplasmsView all (30 more) |
334
|
|
|
Fibroblast growth factor receptor 4 |
CD334, JTK2, TKF |
|
335
|
|
|
Fibroblast growth factor receptor like 1 |
FGFR-5, FGFR5, FHFR |
|
336
|
|
|
Fibrinogen gamma chain |
- |
Blood coagulation disorder, Cardioembolic stroke, Thromboembolic pulmonary hypertension, Congenital afibrinogenemia, Congenital fibrinogen deficiency, Congenital hypofibrinogenemia, Cor pulmonale, Dysfibrinogenemia, Afibrinogenemia, Hypofibrinogenemia, Heart disease, Spastic paraplegia, Stomach neoplasms, Stroke, Thrombocytopenia, Thrombophilia, Venous thromboembolismView all (2 more) |
337
|
|
|
FGGY carbohydrate kinase domain containing |
- |
|
338
|
|
|
Fibrinogen like 1 |
HFREP1, HP-041, HPS, LFIRE-1, LFIRE1 |
|
339
|
|
|
Fibrinogen like 2 |
T49, pT49 |
|
340
|
|
|
FGR proto-oncogene, Src family tyrosine kinase |
SRC2, c-fgr, c-src2, p55-Fgr, p55c-fgr, p58-Fgr, p58c-fgr |
|
