|
311
|
|
|
Rho guanine nucleotide exchange factor 12 |
LARG, PRO2792 |
|
|
312
|
|
|
Rho/Rac guanine nucleotide exchange factor 18 |
P114-RhoGEF, RP78, SA-RhoGEF, p114RhoGEF |
Cataract, Congenital hypoplasia of penis, Cystoid macular edema, Diabetes mellitus, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Leukemia, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosaView all (1 more) |
|
313
|
|
|
Adenosylhomocysteinase like 2 |
ADOHCYASE3, IRBIT2 |
|
|
314
|
|
|
Activity dependent neuroprotector homeobox |
ADNP1, HVDAS, MRD28 |
Accessory kidney, Adnp syndrome, Agenesis of corpus callosum, Anxiety disorder, Astigmatism, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Brachydactyly, Central visual impairment, Cerebral atrophy, Congenital coloboma of iris, Congenital exomphalos, Congenital hypothyroidism, Congenital omphalocele, Cryptorchidism, Developmental delay, Developmental regression, Dwarfism, Dysmorphic features, Dyssomnia, Esotropia, Exotropia, Gastroesophageal reflux disease, Helsmoortel-van der aa syndrome, Hyperopia, Hypoplasia of corpus callosum, Hypothyroidism, Isolated somatotropin deficiency, Language disorders, Macrocephaly, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microtia, Movement disorders, Multiple congenital anomalies, Neurodevelopmental disorders, Obesity, Obsessive-compulsive disorder, Oropharyngeal dysphagia, Patent foramen ovale, Plagiocephaly, Polydactyly, Prostate cancer, Ptosis, Schizophrenia, Sleep disorders, Social communication disorder, Speech disorders, Stereotyped behavior, Strabismus, Syndactyly of the toes, TrigonocephalyView all (40 more) |
|
315
|
|
|
ATPase cation transporting 13A2 |
CLN12, HSA9947, KRPPD, PARK9, SPG78 |
Akinesia, Anarthria speech disorder, Atherosclerotic parkinsonism, Blepharospasm, Bowel incontinence, Cerebellar ataxia, Cerebellar atrophy, Cerebral cortical atrophy, Dementia, Disorder of eye, Dysarthria, Dyskinetic syndrome, Dysmorphic features, Dysphagia, Hallucinations, Horizontal nystagmus, Hypoplasia of corpus callosum, Impaired cognition, Kufor-rakeb syndrome, Mental depression, Neurogenic urinary bladder, Neuronal ceroid lipofuscinosis, Nystagmus, Parkinson disease, Parkinsonian disease, Psychosis, Ramsay hunt paralysis syndrome, Spastic paraplegia, Spastic quadriplegia, Strabismus, Supranuclear gaze palsy, Upgaze palsyView all (17 more) |
|
316
|
|
|
Adaptor related protein complex 4 subunit epsilon 1 |
CPSQ4, SPG51, STUT1 |
Cerebellar atrophy, Cerebral cortical atrophy, Congenital clubfoot, Developmental dysplasia of the hip, Congenital genu recurvatum, Developmental delay, Dwarfism, High palate, Hypoplasia of corpus callosum, Mental retardation, Macrostomia, Mental retardation with spastic paraplegia, Microcephaly, Hypotonia, Nystagmus, Spastic paraplegia, Spastic quadriplegia, Stereotyped behavior, Strabismus, StutteringView all (5 more) |
|
317
|
|
|
ATP binding cassette subfamily B member 10 |
EST20237, M-ABC2, MTABC2 |
|
|
318
|
|
|
ATP binding cassette subfamily B member 9 |
EST122234, TAPL |
|
|
319
|
|
|
ATP binding cassette subfamily A member 6 |
EST155051 |
|
|
320
|
|
|
ATP binding cassette subfamily A member 5 |
ABC13, DEL17q24, EST90625, HTC3, HTGH |
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