|
541
|
|
|
Antioxidant 1 copper chaperone |
ATX1, HAH1 |
|
|
542
|
|
|
ATPase Na+/K+ transporting subunit alpha 1 |
CMT2DD, HOMGSMR2 |
Adenoma, Hyperaldosteronism, Adrenocortical adenoma, Aldosterone-producing adrenal cortex adenoma, Bipolar disorder, Charcot-marie-tooth disease, Conn syndrome, Developmental delay, Gastroenteritis, Hypertension, Hypomagnesemia, Mental retardation, Myocardial infarction, Myocardial ischemia, Papillary adenoma, Seizure, Sensorimotor neuropathy, Status epilepticus, Vestibular diseasesView all (4 more) |
|
543
|
|
|
ATPase Na+/K+ transporting subunit alpha 2 |
DEE98, FARIMPD, FHM2, MHP2 |
Alternating hemiplegia, Aphasia, Apraxia, Arthrogryposis multiplex congenita, Benign epilepsy, Bipolar disorder, Cerebral microangiopathy, Choreoathetosis, Dysarthria, Dysphasia, Epilepsy, Epilepsy and migraine, Epileptic encephalopathy, Episodic ataxia, Episodic quadriplegia, Hearing loss, Hemiplegia/hemiparesis, Hemiplegic migraine, Hydrops fetalis, Hypertension, Hypokalemic periodic paralysis, Malformation of cortical development, Mental retardation, Microcephaly, Migraine, Migraine with aura, Movement disorders, Nystagmus, Polymicrogyria, Retinitis pigmentosa, SeizureView all (16 more) |
|
544
|
|
|
ATPase Na+/K+ transporting subunit alpha 3 |
AHC2, ATP1A1, CAPOS, DEE99, DYT12, RDP |
Alternating hemiplegia, Anhedonia, Anxiety disorder, Arthritis, Autism, Bipolar disorder, Capos syndrome, Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome, Cerebellar atrophy, Cerebral palsy, Choreoathetosis, Congenital epicanthus, Congestive heart failure, Developmental delay, Dysarthria, Dyskinetic syndrome, Dysmorphic features, Dysphagia, Dystonia, Dystonia-parkinsonism, Epilepsy, Epileptic encephalopathy, Episodic ataxia, Episodic quadriplegia, Febrile seizures, Hearing loss, Heart failure, Impaired cognition, Mental depression, Mental retardation, Mood swings, Motor delay, Movement disorders, Multiple congenital anomalies, Myocardial infarction, Nystagmus, Optic atrophy, Osteoarthrosis deformans, Parkinson disease, Parkinsonian disease, Ramsay hunt paralysis syndrome, Sagittal craniosynostosis, Status epilepticus, TaurodontismView all (29 more) |
|
545
|
|
|
Aconitase 1 |
ACONS, HEL60, IREB1, IREBP, IREBP1, IRP1 |
|
|
546
|
|
|
ATPase Na+/K+ transporting subunit alpha 4 |
ATP1A1, ATP1AL2 |
|
|
547
|
|
|
ATPase Na+/K+ transporting subunit beta 1 |
ATP1B |
|
|
548
|
|
|
ATPase Na+/K+ transporting subunit beta 2 |
AMOG |
|
|
549
|
|
|
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1 |
ATP2A, SERCA1 |
|
|
550
|
|
|
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 |
ATP2B, DAR, DD, RHABDO2, SERCA2 |
Acantholytic dyskeratotic epidermal nevus, Acrokeratosis, Acrokeratosis verruciforms, Bipolar disorder, Congestive heart failure, Darier disease, Depressed bipolar disorder, Diabetes mellitus, Diabetic cardiomyopathy, Grand mal status epilepticus, Heart diseases, Heart failure, Hibernation, myocardial, Hyperkeratosis, Hypertrophy of parotid gland, Keratosis follicularis, Major affective disorder, Mental depression, Mental retardation, Mood disorder, Myocardial infarction, Myocardial stunning, Nonconvulsive status epilepticus, Palmoplantar keratoderma, Petit mal status, Schizophrenia, Status epilepticus, Stunned myocardiumView all (13 more) |
