|
111
|
|
|
Potassium voltage-gated channel subfamily A member 2 |
DEE32, EIEE32, HBK5, HK4, HUKIV, KV1.2, MK2, NGK1, RBK2 |
Attention deficit hyperactivity disorder, Auditory processing disorder, Autism, Cerebral atrophy, Clonic seizures, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Hypotonic seizures, Mental retardation, Jacksonian seizure, Language development disorders, Microcephaly, Movement disorders, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Seizure, Speech delay, Status epilepticusView all (10 more) |
|
112
|
|
|
Potassium voltage-gated channel subfamily A member 4 |
HBK4, HK1, HPCN2, HUKII, KCNA4L, KCNA8, KV1.4, MCIDDS, PCN2 |
|
|
113
|
|
|
Potassium voltage-gated channel subfamily A member 5 |
ATFB7, HCK1, HK2, HPCN1, KV1.5, PCN1 |
|
|
114
|
|
|
Potassium voltage-gated channel subfamily A member 10 |
Kcn1, Kv1.8 |
|
|
115
|
|
|
Potassium voltage-gated channel subfamily B member 1 |
DEE26, DRK1, Kv2.1 |
Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Mental depression, Mental retardation, Microcephaly, Myoclonic absences, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Schizophrenia, Status epilepticusView all (5 more) |
|
116
|
|
|
Potassium voltage-gated channel subfamily C member 1 |
EPM7, KV3.1, KV4, NGK2 |
|
|
117
|
|
|
Kinesin family member 7 |
ACLS, AGBK, HLS2, JBTS12, MMEDF, UNQ340 |
Absence of septum pellucidum, Acrocallosal syndrome, Agenesis of corpus callosum, Anencephaly, Arachnoid cyst, Arrhinencephaly, Arthritis, Attention deficit hyperactivity disorder, Bardet-biedl syndrome, Brachydactyly, Brain atrophy, Camptodactyly of fingers, Cerebellar vermis agenesis, Cerebral atrophy, Ciliopathies, Clinodactyly, Colpocephaly, Congenital atresia of trachea, Congenital diaphragmatic hernia, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Congenital malrotation of intestine, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Disorder of eye, Dwarfism, Dysmorphic features, Esotropia, Foot polydactyly, Frontal bossing, Hearing loss, Heart septal defects, High palate, Hydrocephalus, Hydrolethalus syndrome, Hypoplasia of the optic nerve, Hypospadias, Hypothalamic hamartomas, Imperforate anus, Mental retardation, Joubert syndrome, Joubert syndrome, digenic, Laryngomalacia, Macrocephaly, Macrocephaly with multiple epiphyseal dysplasia and distinctive facies, Malformation of cortical development, Micrognathism, Micromelia, Microphthalmos, Motor delay, Multiple congenital anomalies, Multiple epiphyseal dysplasia, Hypotonia, Nystagmus, Obesity, Orofaciodigital syndrome, Polycystic ovary syndrome, Polydactyly, Polydactyly of toes, Ptosis, Radial polydactyly, Renal agenesis, Strabismus, Submucosal cleft palate, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Syndromic microphthalmia, Postaxial hand polydactyly, Uterine anomaliesView all (59 more) |
|
118
|
|
|
Potassium voltage-gated channel subfamily C member 3 |
KSHIIID, KV3.3, SCA13 |
Cerebellar ataxia, Cerebellar atrophy, Developmental delay, Dwarfism, Dysarthria, Dysphagia, Mental retardation, Motor delay, Nystagmus, Optic atrophy, Spinocerebellar ataxia, Upgaze palsy |
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119
|
|
|
Potassium voltage-gated channel subfamily C member 4 |
C1orf30, HKSHIIIC, KSHIIIC, KV3.4 |
|
|
120
|
|
|
Potassium voltage-gated channel subfamily D member 2 |
KV4.2, RK5 |
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