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3241
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Fibroblast growth factor 14 |
FGF-14, FHF-4, FHF4, NYS4, SCA27, SCA27A, SCA27B |
Akinesia, Autism, Cartilage diseases, Cerebellar atrophy, Chondromalacia, Cognitive disorder, Color blindness, Common variable immunodeficiency, Congenital pectus carinatum, Cryptorchidism, Diabetes mellitus, Dysarthria, Dysgraphia, Hyperopia, Impaired cognition, Orofacial dyskinesia, Lung diseases, Mental depression, Mental retardation, Nystagmus, Patent foramen ovale, Scoliosis, Septic toxemia, Spinocerebellar ataxia, Strabismus, Talipes valgus, UranostaphyloschisisView all (12 more) |
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3242
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Aldolase, fructose-bisphosphate A |
ALDA, GSD12, HEL-S-87p |
Anemia, Breast cancer, Mammary neoplasms, Breast carcinoma, Cholecystitis, Cholelithiasis, Congenital epicanthus, Dwarfism, Enzymopathy, Glycogen storage disease, Hemolytic anemia, Lung adenocarcinoma, Marfan syndrome, Myocardial ischemia, Ptosis |
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3243
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Fibroblast growth factor receptor 1 |
BFGFR, CD331, CEK, ECCL, FGFBR, FGFR-1, FLG, FLT-2, FLT2, HBGFR, HH2, HRTFDS, KAL2, N-SAM, OGD, bFGF-R-1 |
8p11 myeloproliferative syndrome, Absence of septum pellucidum, Acquired porencephaly, Acrocephaly, Agenesis of corpus callosum, Alopecia, Ambiguous genitalia, Anaplastic astrocytoma, Elbow ankylosis, Anxiety disorder, Aortic coarctation, Aortic valve sclerosis, Aphasia, Aqueductal stenosis, Arachnoid cyst, Arnold-chiari malformation, Asthma, Astrocytoma, Atrial septal defect, Autism, Bipolar disorder, Brachycephaly, Brachydactyly, Brain stem glioma, Breast adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Bronchomalacia, Carcinoma, Cardiac valvular disease, Cerebellar hypoplasia, Cerebral cortical atrophy, Choanal atresia, Congenital camptodactyly, Congenital cerebral hernia, Congenital coloboma of iris, Congenital epicanthus, Breast hypoplasia, Hypoplasia of the ovary, Congenital hypoplasia of penis, Congenital omphalocele, Congenital sensorineural hearing loss, Coronal craniosynostosis, Cortical dysplasia, Craniofacial dysostosis, Craniosynostosis, Cryptorchidism, Cyclocephaly, Dandy-walker syndrome, Development disorder, Developmental delay, Diabetes insipidus, Duodenal atresia, Dwarfism, Dysarthria, Dysphasia, Dyssomnia, Ectrodactyly, Encephalocraniocutaneous lipomatosis, Erectile dysfunction, Esophageal atresia, Female hypogonadism syndrome, Fgfr2-related craniosynostosis, Fibrillary astrocytoma, Frontal bossing, Fused incisors, Gastric cancer, Gemistocytic astrocytoma, Giant cell glioblastoma, Glioblastoma, Glioma, Gliosarcoma, Gonadotropin deficiency, Grade i astrocytoma, Gynecomastia, Hartsfield syndrome, Head and neck carcinoma, Head and neck neoplasms, Hearing loss, Hemangioma, Hemiplegia/hemiparesis, High palate, Holoprosencephaly, Holoprosencephaly, ectrodactyly, and bilateral cleft lip-palate, Hydrocephalus, Hydronephrosis, Hypodontia, Hypogonadism, Hypogonadotropic hypogonadism, Hypohidrosis, Hypopituitarism, Hypoplasia of corpus callosum, Hypoplasia of iris, Hypoplasia of the maxilla, Hypospadias, Hypothyroidism, Ichthyosis, Infiltrating duct carcinoma of female breast, Interfrontal craniofaciosynostosis, Interrupted aortic arch, Intracranial astrocytoma, Jackson-weiss syndrome, Kallmann syndrome, Lipodystrophy, Lipoma, Liver carcinoma, Lobar holoprosencephaly, Lung carcinoma, Lung neoplasms, Lung cancer, Lymphoblastic leukemia with lymphomatous features, Macrocephaly, Head and neck cancer, Malignant neoplasm, Malocclusion, Marfan syndrome, Meckel diverticulum, Medulloblastoma, Melancholia, Mental depression, Mental retardation, Metopic synostosis, Microcephaly, Microdontia, Microform holoprosencephaly, Micrognathism, Microphthalmos, Mirror movements, Multiple lipomata, Myeloid/lymphoid neoplasm associated with fgfr1 rearrangement, Myeloproliferative disorder, Hypotonia, Neoplasm of skeletal system, Neoplasms, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Oligoastrocytoma, Oligodontia, Osteochondrodysplasia, Osteochondrosis, Osteoglosphonic dysplasia, Osteopenia, Osteoporosis, Panhypopituitarism, Paraplegia, Pelvic kidney, Penis agenesis, Peripheral pulmonary artery stenosis, Pfaundler-hurler syndrome, Pfeiffer syndrome, Pfeiffer type acrocephalosyndactyly, Phakomatosis pigmentovascularis, Physiologic amenorrhea, Pilomyxoid astrocytoma, Polydactyly, Porencephalic cyst, Posteriorly rotated ear, Hypereosinophilic syndrome, Proptosis, Protoplasmic astrocytoma, Ptosis, Pulmonary arterial hypertension, Quadriplegia, Ramer ladda syndrome, Renal agenesis, Retinal diseases, Rhizomelia, Rosette-forming glioneuronal neoplasm, Scaphocephaly, Schizophrenia, Sclerocornea, Scoliosis, Secondary physiologic amenorrhea, Semilobar holoprosencephaly, Septo-optic dysplasia, Skeletal dysplasia, Sleep disorders, Spade-like hand, Strabismus, Strawberry nevus of skin, Subaortic stenosis, Subcortical cerebral atrophy, Subcutaneous lipoma, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Synophrys, Synostotic anterior plagiocephaly, Synostotic posterior plagiocephaly, Talipes transversoplanus, Testicular hypogonadism, Tetralogy of fallot, Bladder carcinoma, Tricuspid valve prolapse, Trigonocephaly, Ventricular septal defect, Visceral angiomatosis, XanthomatosisView all (186 more) |
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3244
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Fibroblast growth factor receptor 3 |
ACH, CD333, CEK2, HSFGFR3EX, JTK4 |
Absent lacrimal punctum, Acanthosis nigricans, Achondroplasia, Achondroplasia with developmental delay and acanthosis nigricans, Acrocephaly, Alacrima, Arachnodactyly, Arnold-chiari malformation, Arthritis, Atrial septal defect, Azoospermia, Benign neoplasm of bladder, Urinary bladder cancer, Bladder neoplasm, Bladder carcinoma, Blepharospasm, Brachycephaly, Brachydactyly, Brain atrophy, Camptodactyly of fingers, Camptodactyly-tall stature-scoliosis-hearing loss syndrome, Carcinoma, Carcinoma of the head and neck, Carpal synostosis, Cerebral atrophy, Uterine cervix neoplasm, Cervix carcinoma, Cervical intraepithelial neoplasia, Cervical cancer, Cervical tumor, Choanal atresia, Choriocarcinoma, Colorectal cancer, Colorectal neoplasms, Congenital cerebral hernia, Congenital epicanthus, Short femur, Congenital hypoplasia of radius, Congenital pectus excavatum, Coronal craniosynostosis, Coronal hypospadias, Craniofacial dysostosis, Craniosynostosis, Crouzon syndrome-acanthosis nigricans syndrome, Cryptorchidism, Dacryocystitis, Dental enamel hypoplasia, Developmental delay, Dwarfism, Dysarthria, Dysmorphic features, Epidermal nevus, Epilepsy, Erosion of cornea, Frontal bossing, Giant cell glioblastoma, Gliosarcoma, Gonadal dysgenesis, Hearing loss, Hereditary nonpolyposis colorectal cancer, Holoprosencephaly, Hydrocephalus, Hypochondroplasia, Hypodontia, Hypoplasia of corpus callosum, Hypoplasia of lower limb, Hypoplasia of the maxilla, Impaired cognition, Inflammatory abnormality of the eye, Mental retardation, Lacrimoauriculodentodigital syndrome, Leiomyosarcoma of uterus, Limbal stem cell deficiency, Lung carcinoma, Lung adenocarcinoma, Lymphoma, Macrocephaly, Malformation of cortical development, Malignant neoplasm of testis, Melanocytic nevus, Mesomelia, Metaphyseal chondrodysplasia, Microcephaly, Micromelia, Microtia, Migraine, Motor delay, Muenke syndrome, Multicystic renal dysplasia, Multiple myeloma, Myeloproliferative disorder, Neoplasms, Nephrosclerosis, Neuronal heterotopia, Nonepidermolytic keratinocytic nevus, Obesity, Optic atrophy, Osteochondrodysplasia, Osteochondroma, Otitis media, Papillary syringocystadenoma, Papillary renal carcinoma, Patent ductus arteriosus, Plagiocephaly, Polydactyly, Brain stem compression, Proptosis, Ptosis, Radial polydactyly, Renal agenesis, Renal aplasia, Renal carcinoma, Rhizomelia, Saddan dysplasia, Saethre-chotzen syndrome, Scoliosis, Seborrheic keratosis, Seizure, Seminoma, Skeletal dysplasia, Skeletal dysplasia with acanthosis nigricans, Sleep apnea, Spermatocytic seminoma, Stomach neoplasms, Strabismus, Syndactyly of fingers, Tarsal coalition, Teratoma, Testicular germ cell tumor, Thanatophoric dysplasiaView all (115 more) |
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3245
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Glypican 5 |
- |
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3246
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Fibroblast growth factor receptor 2 |
BBDS, BEK, BFR-1, CD332, CEK3, CFD1, ECT1, JWS, K-SAM, KGFR, TK14, TK25 |
Absence of septum pellucidum, Absent lacrimal punctum, Acanthosis nigricans, Acne, Acrobrachycephaly, Acrocephalopolydactyly, Acrocephaly, Agenesis of corpus callosum, Alacrima, Antley-bixler syndrome, Apert syndrome, Apert-crouzon disease, Aqueductal stenosis, Arachnodactyly, Arachnoid cyst, Arnold-chiari malformation, Atresia of vagina, Atrial septal defect, Bannayan-riley-ruvalcaba syndrome, Benign neoplasm of stomach, Benign prostatic hyperplasia, Bent bone dysplasia, Bipolar disorder, Blepharospasm, Brachycephaly, Brachydactyly, Breast cancer, Breast carcinoma, Bronchomalacia, Camptodactyly of fingers, Cerebellar hypoplasia, Choanal atresia, Cholangiocarcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital anomaly of limb, Congenital camptodactyly, Congenital coloboma of iris, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Congenital hypoplasia of radius, Congenital keratoglobus, Congenital malrotation of intestine, Congenital nystagmus, Congenital posterior urethral valves, Conjunctivitis, Corneal erosion, Coronal craniosynostosis, Coronal hypospadias, Craniofacial dysostosis, Craniosynostosis, Crouzon disease, Cryptorchidism, Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome, Dacryocystitis, Dental enamel hypoplasia, Dermatologic disorders, Developmental delay, Developmental dyspraxia, Dolichocephaly, Dwarfism, Dysgerminoma, Dysmorphic features, Ectopic anus, Elbow ankylosis, Endometrial adenocarcinoma, Endometrial cancer, Endometrial carcinoma, Endometrial endometrioid adenocarcinoma, variant with squamous differentiation, Endometrial neoplasms, Erosion of cornea, Esophageal atresia, Esophageal carcinoma, Fgfr2-related craniosynostosis, Frontal bossing, Gastric cancer, Glaucoma, congenital, Gout, Gouty arthritis, Hamartoma, Head and neck cancer, Head and neck carcinoma, Head and neck neoplasms, Hearing loss, High palate, Horseshoe kidney, Hydrocephalus, Hydronephrosis, Hypertension, Hypertrophy of clitoris, Hypodontia, Hypoplasia of the maxilla, Imperforate anus, Intrahepatic cholangiocarcinoma, Jackson-weiss syndrome, Keratitis, Lacrimoauriculodentodigital syndrome, Laryngomalacia, Lhermitte-duclos disease, Limbal stem cell deficiency, Liver cirrhosis, Liver fibrosis, Lung adenocarcinoma, Lung cancer, Lung carcinoma, Lung neoplasms, Macrocephaly, Macrotia, Malignant uterine corpus neoplasm, Malocclusion, Mammary neoplasms, Marfan syndrome, Melanocytic nevus, Mental depression, Mental retardation, Metopic synostosis, Micrognathism, Micromelia, Microstomia, Microtia, Migraine, Motor skills disorders, Multiple congenital anomalies, Nasopharyngeal carcinoma, Nasopharyngeal neoplasms, Nephrosclerosis, Night blindness, Nonorganic psychosis, Odontome, Oestrogen receptor positive breast cancer, Optic atrophy, Osteopenia, Otitis media, Ovarian endometrioid carcinoma, Ovarian neoplasm, Ovarian serous adenocarcinoma, Overriding aorta, Palmoplantar keratoderma, Parietal foramina, Pfeiffer syndrome, Pfeiffer type acrocephalosyndactyly, Plagiocephaly, Polydactyly, Proptosis, Prostate cancer, Psychosis, Pten hamartoma tumor syndrome, Ptosis, Rachischisis, Radial polydactyly, Radioulnar synostosis, Ramer ladda syndrome, Renal agenesis, Saethre-chotzen syndrome, Sagittal craniosynostosis, Scaphocephaly, Scaphocephaly, maxillary retrusion, and mental retardation, Schizophrenia, Scoliosis, Short clavicles, Sleep apnea, Spina bifida, Split hand foot deformity, Status dysraphicus, Stenosis of external auditory canal, Stomach carcinoma, Stomach neoplasms, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Synophrys, Synostotic anterior plagiocephaly, Synostotic posterior plagiocephaly, Talipes, Tracheomalacia, Trigonocephaly, Ventricular septal defect, Vertical talus, Vesicoureteral reflux, Visceral angiomatosisView all (167 more) |
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3247
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Fibroblast growth factor receptor 4 |
CD334, JTK2, TKF |
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3248
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Fibrinogen gamma chain |
- |
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3249
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Fibrinogen like 1 |
HFREP1, HP-041, HPS, LFIRE-1, LFIRE1 |
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3250
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Fumarate hydratase |
FMRD, HLRCC, HsFH, LRCC, MCL, MCUL1 |
Adrenal gland pheochromocytoma, Agenesis of corpus callosum, Aniridia, Barrett esophagus, Breast carcinoma, Hereditary cancer syndrome, Capillary hemangioma of retina, Carcinoma, Cataract, Cerebral atrophy, Cholestasis, Congestive heart failure, Cranial nerve compression, Cutaneous leiomyoma, Developmental delay, Endometrial carcinoma, Episodic paroxysmal anxiety, Extra-adrenal pheochromocytoma, Frontal bossing, Fumarase deficiency, Glomerulonephritis, Glomerulosclerosis, Hearing loss, Hereditary leiomyomatosis and renal cancer, Hereditary paraganglioma-pheochromocytoma syndromes, Hereditary pheochromocytoma-paraganglioma, High palate, Hyperbilirubinemia, Hypercalcemia, Hypertensive retinopathy, Kidney neoplasm, Kidney cancer, Leiomyosarcoma of uterus, Liver failure, Macrocephaly, Microcephaly, Optic atrophy, Panic disorder, Papillary renal carcinoma, Paraganglioma of head and neck, Pheochromocytoma, Polycythemia, Polymicrogyria, Pulsatile tinnitus, Renal carcinoma, Sinus tachycardia, Speech disorders, Status epilepticus, Uterine fibroids, Vaginal neoplasms, Vocal cord paralysisView all (36 more) |
