|
271
|
|
|
Family with sequence similarity 86 member B3, pseudogene |
- |
|
|
272
|
|
|
Family with sequence similarity 83 member H |
AI3, AI3A |
|
|
273
|
|
|
FLVCR choline and heme transporter 1 |
AXPC1, FLVCR, MFSD7B, NEDMISH, PCA, PCARP, RETSNS, SLC49A1 |
Achalasia, Asthma, Bowel incontinence, Cataract, Congenital camptodactyly, Developmental delay, Disorder of eye, Jeune thoracic dystrophy, Liver carcinoma, Mental retardation, Movement disorders, Nyctalopia, Optic atrophy, Osteomyelitis, Posterior column ataxia-retinitis pigmentosa syndrome, Retinitis pigmentosa, Rod-cone dystrophy, Scoliosis, Short rib-polydactyly syndromeView all (4 more) |
|
274
|
|
|
Fascin actin-bundling protein 3 |
- |
|
|
275
|
|
|
Forkhead box A1 |
HNF3A, TCF3A |
|
|
276
|
|
|
Forkhead box A2 |
HNF-3-beta, HNF3B, TCF3B |
|
|
277
|
|
|
Forkhead box A3 |
FKHH3, HNF3G, TCF3G |
|
|
278
|
|
|
Family with sequence similarity 149 member B1 |
JBTS36, KIAA0974 |
Brachydactyly, Cerebellar vermis agenesis, Clinodactyly, Congenital epicanthus, Congenital heart defects, Cryptorchidism, Developmental delay, Dwarfism, Esotropia, Frontal bossing, Hearing loss, High palate, Hypothalamic hamartomas, Malformation of cortical development, Mental retardation, Micrognathism, Nystagmus, Orofaciodigital syndrome, Polydactyly of toes, Radial polydactyly, Renal agenesis, SyndactylyView all (7 more) |
|
279
|
|
|
Free fatty acid receptor 4 |
BMIQ10, GPR120, GPR129, GT01, O3FAR1, OB10Q, PGR4 |
|
|
280
|
|
|
FRAS1 related extracellular matrix 2 |
CRYPTOP, FRASRS2 |
Abnormal spinal segmentation, Ambiguous genitalia, Atresia of vagina, Complete cryptophthalmia, Congenital ankyloblepharon, Congenital cerebral hernia, Congenital diaphragmatic hernia, Congenital exomphalos, Pulmonary hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Congenital pectus excavatum, Cryptophthalmos, Cryptorchidism, Cryptotia, Developmental delay, Diaphragmatic eventration, Disorder of eye, Ectopic anus, Female pseudohermaphroditism, Fraser syndrome, Glaucoma, Hearing loss, High palate, Hydronephrosis, Hypospadias, Imperforate anus, Lacrimal duct aplasia, Laryngostenosis, Marles greenberg persaud syndrome, Meningomyelocele, Mental retardation, Microcephaly, Microphthalmos, Microstomia, Microtia, Multicystic renal dysplasia, Narcolepsy, Patent ductus arteriosus, Polydactyly, Renal agenesis, Renal aplasia, Renal hypoplasia, Schizophrenia, Syndactyly of fingers, Syndactyly of the toes, Syndromic microphthalmia, Tracheal stenosis, Urethral atresia, Ventricular septal defectView all (35 more) |
