Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4671 to 4680 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4671
Fibroblast growth factor receptor like 1
FGFR-5, FGFR5, FHFR
Atrial fibrillation, Bone fracture, Congenital diaphragmatic hernia, Gout, Obesity, Diabetes mellitus type 2, Wolf-hirschhorn syndrome

4672
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
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4673
FGGY carbohydrate kinase domain containing
-
Astrocytoma, Bipolar disorder, Bronchopneumonia, Central nervous system cancer, Dementia, Glioma, Major depressive disorder, Obesity

4674
Fibrinogen like 1
HFREP1, HP-041, HPS, LFIRE-1, LFIRE1
Oligodendroglioma, Preeclampsia

4675
Fibrinogen like 2
T49, pT49
Allergic contact dermatitis

4676
FGR proto-oncogene, Src family tyrosine kinase
SRC2, c-fgr, c-src2, p55-Fgr, p55c-fgr, p58-Fgr, p58c-fgr
Psoriasis, Squamous cell carcinoma

4677
Fumarate hydratase
FMRD, HLRCC, HsFH, LRCC, MCL, MCUL1
Leiomyosarcoma, Major depressive disorder, Pheochromocytoma/paraganglioma syndrome

4678
Forkhead associated phosphopeptide binding domain 1
-
Color vision deficiency, Coronary aneurysm, Iga nephropathy, Pelvic organ prolapse

4679
FH2 domain containing 1
INF1
Amyotrophic lateral sclerosis, Obesity, Oligodendroglioma, Thyrotoxic periodic paralysis

4680
FHF complex subunit HOOK interacting protein 1A
FAM160A1, FHIP-L
Attention deficit hyperactivity disorder, Autism, Dyslexia, Insomnia, Intracerebral hemorrhage, Myopia