|
361
|
|
|
FAT atypical cadherin 4 |
CDHF14, CDHR11, FAT-J, FATJ, HKLLS2, NBLA00548, VMLDS2 |
Adenocarcinoma, Agenesis of corpus callosum, Benign neoplasm of nervous system, Blepharophimosis, Carcinoma, Cerebrofacioarticular syndrome, Choanal atresia, Clinodactyly, Congenital arteriovenous malformation, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Congenital heart defects, Short clavicles, Craniosynostosis, Cryptorchidism, Cystic kidney disease, Developmental delay, Dwarfism, Dysplastic corpus callosum, Ectopic kidney, Erysipelas, Esophagus neoplasm, Gastric cancer, Glaucoma, Hearing loss, Hennekam lymphangiectasia-lymphedema syndrome, Hennekam syndrome, High palate, Horseshoe kidney, Hydrops fetalis, Hypoplasia of corpus callosum, Hypoplasia of the maxilla, Hypospadias, Mental retardation, Lymphangioma, Lymphopenia, Malabsorption syndrome, Melanoma, Microcephaly, Micrognathism, Microstomia, Microtia, Neuronal heterotopia, Osteochondrodysplasia, Osteopenia, Pachygyria, Penis agenesis, Pericardial effusion, Periventricular heterotopia, Periventricular gray matter heterotopia, Periventricular nodular heterotopia, Ptosis, Pulmonary stenosis, Renal hypoplasia, Scoliosis, Skeletal dysplasia, Stomach neoplasms, Subcortical band heterotopia, Syndactyly, Syndactyly of fingers, TracheomalaciaView all (47 more) |
|
362
|
|
|
FAST kinase domains 1 |
- |
|
|
363
|
|
|
Frizzled class receptor 3 |
Fz-3 |
|
|
364
|
|
|
F-box protein 31 |
FBX14, FBXO14, Fbx31, MRT45, pp2386 |
Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Stereotyped behaviorView all (4 more) |
|
365
|
|
|
F-box and leucine rich repeat protein 18 |
Fbl18 |
|
|
366
|
|
|
Fraser extracellular matrix complex subunit 1 |
FRASRS1 |
Abnormal spinal segmentation, Absent eyebrow, Ambiguous genitalia, Atresia of vagina, Congenital atresia of larynx, Congenital cerebral hernia, Congenital diaphragmatic hernia, Congenital exomphalos, Congenital heart defects, Pulmonary hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Congenital pectus excavatum, Cryptophthalmos, Cryptorchidism, Diaphragmatic eventration, Disorder of eye, Ectopic anus, Female pseudohermaphroditism, Fraser syndrome, Hearing loss, High palate, Hydrocephalus, Hydronephrosis, Hypertrophy of clitoris, Hypospadias, Immunodeficiency, Imperforate anus, Lacrimal duct aplasia, Laryngeal web, Laryngostenosis, Macrostomia, Meningomyelocele, Mental retardation, Microcephaly, Microphthalmos, Microtia, Multicystic renal dysplasia, Ovarian neoplasm, Penis agenesis, Polydactyly, Renal agenesis, Renal aplasia, Renal hypoplasia, Syndactyly of fingers, Syndactyly of the toes, Syndromic microphthalmia, Tracheal stenosis, Urethral atresia, Ventricular septal defectView all (35 more) |
|
367
|
|
|
Fuzzy planar cell polarity protein |
CPLANE3, FY, NTD |
Acrania, Ambiguous genitalia, Anencephaly, Arnold-chiari malformation, Arrhinencephaly, Bowel incontinence, Caudal regression sequence, Cervical spina bifida aperta, Cervical spina bifida cystica, Cervicothoracic spina bifida, Chiari malformation, Congenital clubfoot, Pulmonary hypoplasia, Craniorachischisis, Cryptorchidism, Diastematomyelia, Double ureter, Ectopic kidney, Hydrocephalus, Hypertension, Imperforate anus, Lipoma, Lumbosacral spina bifida aperta, Lumbosacral spina bifida cystica, Majewski syndrome, Meningomyelocele, Multiple lipomata, Neural tube defect, Neurenteric cyst, Oral cleft, Primary tethered cord syndrome, Renal agenesis, Renal insufficiency, Sacral agenesis, Scoliosis, Spina bifida, Spina bifida cystica, Spina bifida occulta, Spinal cord myelodysplasia, Thoracolumbosacral spina bifida aperta, Thoracolumbosacral spina bifida cystica, Upper thoracic spina bifida aperta, Upper thoracic spina bifida cystica, Vesicoureteral refluxView all (29 more) |
|
368
|
|
|
F-box protein 11 |
FBX11, IDDFBA, PRMT9, UBR6, UG063H01, VIT1 |
Adenocarcinoma of colon, Brain neoplasms, Breast cancer, Hereditary cancer syndrome, Clinodactyly, Colonic neoplasms, Colorectal neoplasms, Colorectal cancer, Developmental delay, Diffuse lymphoma, Endometrial carcinoma, Gaucher disease, Hereditary nonpolyposis colorectal cancer, Hyperopia, Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, Small intestine cancer, Mental retardation, Microcephaly, Microstomia, Microtia, Ovarian neoplasm, Plagiocephaly, Polyp of large intestine, Posteriorly rotated ear, Small intestinal carcinoma, Strabismus, Turcot syndromeView all (12 more) |
|
369
|
|
|
Formin homology 2 domain containing 3 |
CMH28, FHOS2, Formactin2 |
|
|
370
|
|
|
Flavin adenine dinucleotide synthetase 1 |
FAD1, FADS, LSMFLAD, PP591 |
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