|
801
|
|
|
Triadin |
CARDAR, CPVT5, TDN, TRISK |
Catecholaminergic polymorphic ventricular tachycardia, Diabetes mellitus, Diabetic foot, Dysautonomia, Heart failure, Hereditary and idiopathic neuropathy, Neuropathy, Romano-ward syndrome, Torsades de pointes, Ventricular tachycardia, Ventricular tachycardia, with or without muscle weakness |
|
802
|
|
|
ATP binding cassette subfamily A member 7 |
ABCA-SSN, ABCX, AD9 |
Alzheimer disease, Aphasia, Cerebral cortical atrophy, Dysgraphia, Hallucinations, Language disorders, Mental depression, Mental retardation, Oculomotor apraxia, Oculovestibuloauditory syndrome, Parkinson disease, Semantic dementia, Senile dementia, Senile plaques |
|
803
|
|
|
ATP binding cassette subfamily A member 10 |
EST698739 |
|
|
804
|
|
|
ATP binding cassette subfamily A member 9 |
EST640918 |
|
|
805
|
|
|
ATP binding cassette subfamily A member 8 |
- |
|
|
806
|
|
|
Tryptophanyl tRNA synthetase 2, mitochondrial |
NEMMLAS, PKDYS3, TrpRS, mtTrpRS |
Absence of septum pellucidum, Alopecia, Autism, Central visual impairment, Cerebellar atrophy, Cerebral atrophy, Combined oxidative phosphorylation deficiency, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Exotropia, Hypoglycemia, Hypoplasia of corpus callosum, Mental retardation, Liver failure, Mental depression, Microcephaly, Motor delay, Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, Nystagmus, Optic atrophy, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Spastic quadriplegia, Stereotyped behaviorView all (13 more) |
|
807
|
|
|
Cysteine dioxygenase type 1 |
CDO-I |
|
|
808
|
|
|
Nucleophosmin/nucleoplasmin 3 |
PORMIN, TMEM123 |
|
|
809
|
|
|
High mobility group 20A |
HMGX1, HMGXB1 |
|
|
810
|
|
|
KLF transcription factor 2 |
LKLF |
|
