201
|
|
|
Cholinergic receptor nicotinic alpha 5 subunit |
LNCR2 |
Anxiety disorder, Chronic obstructive pulmonary disease, Clonic seizures, Development disorder, Hypotonic seizures, Jacksonian seizure, Lung carcinoma, Lung neoplasms, Lung adenocarcinoma, Lung cancer, Schizophrenia, Seizure |
202
|
|
|
Cholinergic receptor nicotinic alpha 7 subunit |
CHRNA7-2, NACHRA7, nAChR7 |
15q13.3 microdeletion syndrome, Alzheimer disease, Attention deficit hyperactivity disorder, Auditory processing disorder, Autism, Bipolar disorder, Camptodactyly of fingers, Clonic seizures, Congenital epicanthus, Congenital exomphalos, Congenital omphalocele, Developmental delay, Dwarfism, Epilepsy, Epilepsy with tonic-clonic seizures, Frontal bossing, Hypotonic seizures, Jacksonian seizure, Leukemia, Lung neoplasms, Lung cancer, Macrocephaly, Macrotia, Major affective disorder, Melanocytic nevus, Memory disorders, Age-related memory disorders, Mental retardation, Microcephaly, Nonconvulsive seizure disorder, Schizophrenia, Seizure, Senile dementia, Spina bifida cystica, Spina bifida, StrabismusView all (21 more) |
203
|
|
|
Cholinergic receptor nicotinic beta 1 subunit |
ACHRB, CHRNB, CMS1D, CMS2A, CMS2C, SCCMS |
Myasthenic syndrome, Developmental delay, Facial paralysis, High palate, Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency, Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency, Myopathy, Hypotonia, Ptosis, Respiratory failure |
204
|
|
|
Cholinergic receptor nicotinic beta 2 subunit |
EFNL3, nAChRB2 |
Alzheimer disease, Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Dysmorphic features, Epilepsy, Minimal brain dysfunction, Nocturnal epilepsy, Schizophrenia, Senile dementia, Short sleeper syndromes, Sleep disorders, Sleep wake disorders |
205
|
|
|
Cholinergic receptor nicotinic beta 3 subunit |
- |
|
206
|
|
|
Cholinergic receptor nicotinic beta 4 subunit |
- |
Chronic obstructive pulmonary disease, Clonic seizures, Coronary artery disease, Coronary heart disease, Hypotonic seizures, Jacksonian seizure, Lung neoplasms, Lung carcinoma, Lung adenocarcinoma, Lung cancer, Seizure |
207
|
|
|
Cholinergic receptor nicotinic delta subunit |
ACHRD, CMS2A, CMS3A, CMS3B, CMS3C, FCCMS, SCCMS |
Akinesia, Aplasia of muscle, Breast cancer, Congenital epicanthus, Myasthenic syndrome, Pulmonary hypoplasia, Developmental delay, Dysphagia, Facial paralysis, High palate, Lethal multiple pterygium syndrome, Cystic hygroma, Micrognathism, Multiple pterygium syndrome, Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency, Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency, Myopathy, Hypotonia, Pena shokeir syndrome, Ptosis, Respiratory failureView all (6 more) |
208
|
|
|
Cholinergic receptor nicotinic epsilon subunit |
ACHRE, CMS1A1, CMS1D, CMS1E, CMS2A, CMS4A, CMS4B, CMS4C, FCCMS, FIM1, FIMG, FIMG1, MGI, SCCMS |
Arthrogryposis multiplex congenita, Bernard soulier syndrome, Bulbar palsy, Myasthenic syndrome, Developmental delay, Dysarthria, Dysphagia, Facial paralysis, High palate, Macrothrombocytopenia, Malocclusion, Motor delay, Myasthenia gravis, Myopathy, Hypotonia, Ptosis, Respiratory failure, Strabismus, Sudden episodic apnea, Von willebrand disorderView all (5 more) |
209
|
|
|
Cholinergic receptor nicotinic gamma subunit |
ACHRG |
Abnormal spinal segmentation, Akinesia, Aortic aneurysm, Aplasia of muscle, Arachnodactyly, Arthrogryposis multiplex congenita, Bone disease, Congenital alveolar dysplasia, Camptodactyly, Congenital anomaly of neck, Congenital clubfoot, Congenital diaphragmatic hernia, Dislocated radial head, Congenital epicanthus, Congenital exomphalos, Rib fusion, Pulmonary hypoplasia, Congenital hypoplasia of penis, Myasthenic syndrome, Congenital pectus excavatum, Cryptorchidism, Diaphragmatic eventration, Dolichocephaly, Dwarfism, Dysmorphic features, Exostosis of external ear canal, Hearing loss, High palate, Hypogonadism, Hypoplasia of nipple, Hypospadias, Impaired cognition, Lethal multiple pterygium syndrome, Cystic hygroma, Microcephaly, Micrognathism, Microstomia, Multiple congenital anomalies, Multiple pterygium syndrome, Neck webbing, Nevus, Pena shokeir syndrome, Peripheral neuropathy, Pterygium, Ptosis, Scoliosis, Spina bifida occulta, Strabismus, Syndactyly, Syndactyly of fingers, Vertical talusView all (36 more) |
210
|
|
|
Component of inhibitor of nuclear factor kappa B kinase complex |
BPS2, IKBKA, IKK-1, IKK-alpha, IKK1, IKKA, NFKBIKA, TCF16 |
Bone disease, Cocoon syndrome, Anotia, Mandibular aplasia, Congenital anomaly of limb, Congenital omphalocele, Diabetes mellitus, Embryopathy, Fetal diseases, Fetal encasement syndrome, Hypoplasia of lower limb, Microcephaly, Multiple congenital anomalies |