|
351
|
|
|
Forkhead box L2 |
BPES, BPES1, PFRK, PINTO, POF3 |
Blepharophimosis, Blepharophimosis, ptosis, and epicanthus inversus syndrome, Blepharophimosis, ptosis, and epicanthus inversus syndrome with duane retraction syndrome, Blepharophimosis, ptosis, and epicanthus inversus syndrome with ovarian failure, Blepharophimosis, ptosis, and epicanthus inversus syndrome without ovarian failure, Colorectal cancer, Colorectal neoplasms, Granulosa cell tumor, High palate, Hyperopia, Maligant granulosa cell tumor of the ovary, Maligant granulosa cell tumor of ovary, Microcornea, Microphthalmos, Nystagmus, Ovarian tumor, Premature menopause, Premature ovarian failure, Ovarian failure, Ptosis, Secondary physiologic amenorrhea, StrabismusView all (7 more) |
|
352
|
|
|
Formin like 1 |
C17orf1, C17orf1B, FHOD4, FMNL, KW-13 |
|
|
353
|
|
|
Frizzled class receptor 5 |
C2orf31, HFZ5, MCOPCB11 |
|
|
354
|
|
|
FTO alpha-ketoglutarate dependent dioxygenase |
ALKBH9, BMIQ14, GDFD, IFEX9 |
Allergic rhinitis, Atrial fibrillation, Brachydactyly, Breast cancer, Mammary neoplasms, Breast carcinoma, Cardiovascular diseases, Childhood obesity, Chronic obstructive pulmonary disease, Congenital exomphalos, Coronary heart disease, Cryptorchidism, Cutis marmorata, Dandy-walker syndrome, Developmental delay, Diabetes, Diabetes mellitus, Hearing loss, Heart failure, Hydrocephalus, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Kidney failure, Knee osteoarthritis, Lethal polymalformative syndrome, Leukopenia, Lissencephaly, Macroglossia, Malignant melanoma of skin, Malignant neoplasm, Marfan syndrome, Melanoma, Mental depression, Metabolic syndrome, Microcephaly, Mood disorder, Obesity, Osteoarthritis of hip, Patent ductus arteriosus, Rheumatoid arthritis, Stroke, Urolithiasis, Ventricular septal defectView all (28 more) |
|
355
|
|
|
FAST kinase domains 3 |
- |
|
|
356
|
|
|
Fukutin related protein |
FKTR, LGMD2I, LGMDR9, MDC1C, MDDGA5, MDDGB5, MDDGC5 |
Absence of septum pellucidum, Acquired kyphoscoliosis, Agenesis of corpus callosum, Agyria, Alpha-dystroglycanopathy, Amyotrophy, Anterior segment dysgenesis, Arachnodactyly, Cardiomyopathy, Cataract, Cerebellar atrophy, Cerebellar hypoplasia, Cerebral cortical atrophy, Cobblestone lissencephaly, Congenital coloboma of iris, Congenital contracture, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital kyphoscoliosis, Congenital meningocele, Congenital muscular dystrophy, Congenital muscular dystrophy with cerebellar involvement, Congenital muscular dystrophy with intellectual disability, Congenital muscular dystrophy without intellectual disability, Congenital ocular coloboma, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Diabetes mellitus, Facial paralysis, Fukuyama type congenital muscular dystrophy, Glaucoma, Glaucoma, congenital, Hemiplegia/hemiparesis, Holoprosencephaly, Hydrocephalus, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Impaired cognition, Imperforate anus, Mental retardation, Left ventricular hypertrophy, Lymphocytic leukemia, Limb-girdle muscle atrophy, Limb-girdle muscular dystrophy, Limb-girdle muscular dystrophy-dystroglycanopathy, Macrocephaly, Macroglossia, Meningoencephalocele, Microcephaly, Microcornea, Microphthalmos, Microtia, Motor delay, Muscle eye brain disease, Muscular dystrophy, Muscular dystrophy-dystroglycanopathy, Myopathy, Myopia, Nasopharyngeal carcinoma, Hypotonia, Neuronal heterotopia, Occipital encephalocele, Optic atrophy, Pachygyria, Penis agenesis, Polymicrogyria, Posteriorly rotated ear, Renal dysplasia, Respiratory failure, Retinal detachment, Retinal dysplasia, Retinal dystrophy, Retinitis pigmentosa, Scoliosis, Specific learning disorder, Speech disorders, Strabismus, Submucosal cleft palate, Syndromic microphthalmia, Walker-warburg congenital muscular dystrophy, Walker-warburg syndromeView all (67 more) |
|
357
|
|
|
Fatty acid 2-hydroxylase |
FAAH, FAH1, FAXDC1, SCS7, SPG35 |
Anarthria speech disorder, Anxiety disorder, Atrophy of corpus callosum, Atrophy of the spinal cord, Bipolar disorder, Bowel incontinence, Brainstem atrophy, Broca aphasia, Cerebellar atrophy, Cerebral cortical atrophy, Developmental regression, Dysarthria, Dysmyelinating leukodystrophy and spastic paraparesis with or without dystonia, Dysphagia, Fatty acid hydroxylase associated neurodegeneration, Focal seizures, Horizontal nystagmus, Hypoplasia of corpus callosum, Impaired cognition, Major affective disorder, Maternal hypertension, Mental depression, Mental retardation, Nervous system diseases, Neurogenic urinary bladder, Nocturnal enuresis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Seizure, Spastic paraplegia, Spastic tetraparesis, StrabismusView all (19 more) |
|
358
|
|
|
Fibronectin type III and SPRY domain containing 1 |
GLFND, MIR1 |
|
|
359
|
|
|
FYVE and coiled-coil domain autophagy adaptor 1 |
CATC2, CTRCT18, RUFY3, ZFYVE7 |
|
|
360
|
|
|
Family with sequence similarity 184 member A |
C6orf60 |
|
