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3221
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Aldehyde dehydrogenase 3 family member A2 |
ALDH10, FALDH, SLS |
Central nervous system demyelination, Corneal erosion, Dental enamel hypoplasia, Dwarfism, Dysarthria, Hyperkeratosis, Ichthyosis, Inflammatory abnormality of the eye, Spastic diplegia, Age-related macular degeneration, Mental retardation, Microcephaly, Myopia, Osteochondrodysplasia, Retinal diseases, Scoliosis, Sjogren-larsson syndrome, Skeletal dysplasia, UrticariaView all (4 more) |
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3222
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FER tyrosine kinase |
PPP1R74, TYK3, p94-Fer |
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3223
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FES proto-oncogene, tyrosine kinase |
FPS |
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3224
|
|
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Fibrinogen alpha chain |
AMYLD2, Fib2 |
Afibrinogenemia, Amyloidosis, Cholestasis, Complement component deficiency, Congenital dysfibrinogenemia, Congenital hypodysfibrinogenemia, Congenital afibrinogenemia, Dysfibrinogenemia, Fibrinogen a alpha-chain amyloidosis, Fibrinogen deficiency, Hypertension, Hypodysfibrinogenemia, Hypofibrinogenemia, Kidney disease, Mouth neoplasms, Malignant neoplasm of mouth, Nephrotic syndrome, Osteoporosis, Pulmonary thromboembolism, Stroke, ThrombophiliaView all (6 more) |
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3225
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|
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Fibrinogen beta chain |
HEL-S-78p |
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3226
|
|
|
FYVE, RhoGEF and PH domain containing 1 |
AAS, FGDY, MRXS16, ZFYVE3 |
Aarskog syndrome, Aarskog-scott syndrome, Anencephaly, Attention deficit hyperactivity disorder, Brachydactyly, Camptodactyly of fingers, Clinodactyly, Congenital epicanthus, Congenital exomphalos, Congenital deformity of foot, Congenital genu recurvatum, Congenital keratoglobus, Congenital pectus excavatum, Congestive heart failure, Cryptorchidism, Drachtman weinblatt sitarz syndrome, Dwarfism, Dysmorphic features, Faciodigitogenital syndrome, Hyperopia, Hypodontia, Hypoplasia of the maxilla, Impaired cognition, Mental retardation, Mental retardation, x-linked, Minimal brain dysfunction, Multiple congenital anomalies, Ptosis, Scoliosis, Spade-like hand, Strabismus, Syndactyly, Syndactyly of fingers, Talipes, Talipes transversoplanus, Urogenital abnormalitiesView all (21 more) |
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3227
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|
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Fibroblast growth factor 1 |
AFGF, ECGF, ECGF-beta, ECGFA, ECGFB, FGF-1, FGF-alpha, FGFA, GLIO703, HBGF-1, HBGF1 |
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3228
|
|
|
Fibroblast growth factor 2 |
BFGF, FGF-2, FGFB, HBGF-2 |
Alveolitis, Brain infarction, Clonic seizures, Corneal neovascularization, Cryptogenic tonic-clonic epilepsy, Epilepsy, Glioma, Hypotonic seizures, Jacksonian seizure, Kidney disease, Liver cirrhosis, Liver fibrosis, Melancholia, Mental depression, Mesothelioma, Mood disorder, Myocardial ischemia, Nephrosclerosis, Nephrotic syndrome, Oral submucous fibrosis, Periapical periodontitis, Periodontitis, Prostatic neoplasms, Prostate cancer, Pulmonary fibrosis, Schizophrenia, Seizure, Thrombocythemia, Thrombocytosis, Tonic-clonic epilepsyView all (15 more) |
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3229
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|
|
Fibroblast growth factor 3 |
HBGF-3, INT2 |
Breast adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Cataract, Congenital aplasia of inner ear, Congenital coloboma of iris, Deafness, Deafness with labyrinthine aplasia microtia and microdontia, Dental diseases, Dental pulp stone, Developmental delay, Fundus coloboma, Hearing loss, High-frequency sensorineural hearing impairment, Hypodontia, Lens coloboma, Liver carcinoma, Marfan syndrome, Microcornea, Microdontia, Micrognathism, Microphthalmos, Microtia, Oculootodental syndrome, Odontoma, Otitis media, Otodental syndrome, Peg-shaped teeth, Periodontitis, Retinal coloboma, Stomatognathic diseases, Strabismus, Synophrys, TaurodontismView all (20 more) |
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3230
|
|
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Fibroblast growth factor 4 |
FGF-4, HBGF-4, HST, HST-1, HSTF-1, HSTF1, K-FGF, KFGF, SRTD22 |
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