|
121
|
|
|
Fc gamma receptor IIIb |
CD16, CD16-I, CD16A, CD16b, FCG3, FCGR3, FCGR3A, FCR-10, FCRIII, FCRIIIb |
Alloimmune neutropenia, Compensatory hyperinsulinemia, Dermatitis, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Granulomatosis with polyangiitis, Hyperglycemia, Hyperinsulinism, Lupus erythematosus, Lupus meningoencephalitis, Lupus nephritis, Central nervous system lupus, Neuropsychiatric systemic lupus erythematosus, Obesity, Systemic lupus erythematosus |
|
122
|
|
|
Fukutin |
CMD1X, FCMD, LGMD2M, LGMDR13, MDDGA4, MDDGB4, MDDGC4 |
Absence of septum pellucidum, Acquired kyphoscoliosis, Agenesis of corpus callosum, Agyria, Alpha-dystroglycanopathy, Amyotrophy, Anterior segment dysgenesis, Atrial septal defect, Brachycephaly, Breast cancer, Cardiomyopathy, Cataract, Cerebellar atrophy, Cerebellar hypoplasia, Cobblestone lissencephaly, Congenital cerebral hernia, Congenital coloboma of iris, Congenital contracture, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital kyphoscoliosis, Congenital meningocele, Congenital muscular dystrophy, Congenital muscular dystrophy without intellectual disability, Congenital ocular coloboma, Congenital pectus excavatum, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Dilated cardiomyopathy, Dolichocephaly, Fukuyama type congenital muscular dystrophy, Glaucoma, Glaucoma, congenital, Hearing loss, Hemiplegia/hemiparesis, Holoprosencephaly, Hydrocephalus, Hyperopia, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Impaired cognition, Imperforate anus, Mental retardation, Limb-girdle muscle atrophy, Limb-girdle muscular dystrophy, Limb-girdle muscular dystrophy-dystroglycanopathy, Lipoatrophy, Lipodystrophy, Macrocephaly, Meningoencephalocele, Microcephaly, Microcornea, Microphthalmos, Microtia, Motor delay, Muscle eye brain disease, Muscular dystrophy, Muscular dystrophy-dystroglycanopathy, Myopathy, Myopia, Hypotonia, Neuronal heterotopia, Occipital encephalocele, Optic atrophy, Pachygyria, Palmoplantar keratoderma, Plagiocephaly, Polymicrogyria, Posteriorly rotated ear, Pulmonary stenosis, Renal dysplasia, Retinal detachment, Retinal dysplasia, Retinal dystrophy, Scoliosis, Specific learning disorder, Speech disorders, Strabismus, Submucosal cleft palate, Syndromic microphthalmia, Transposition of great vessels, Walker-warburg congenital muscular dystrophy, Walker-warburg syndromeView all (69 more) |
|
123
|
|
|
Ficolin 1 |
FCNM |
|
|
124
|
|
|
Forkhead box K1 |
FOXK1L |
|
|
125
|
|
|
Ficolin 2 |
EBP-37, FCNL, P35, ficolin-2 |
|
|
126
|
|
|
Farnesyl-diphosphate farnesyltransferase 1 |
DGPT, ERG9, SQS, SQSD, SS |
|
|
127
|
|
|
Family with sequence similarity 185 member A |
- |
|
|
128
|
|
|
F-box and leucine rich repeat protein 13 |
CFAP169, DRC6, Fbl13 |
|
|
129
|
|
|
Farnesyl diphosphate synthase |
FPPS, FPS, POROK9 |
|
|
130
|
|
|
Fer3 like bHLH transcription factor |
N-TWIST, NATO3, NTWIST, PTFB, bHLHa31 |
|
