|
551
|
|
|
Centrosomal protein 112 |
CCDC46, MACOCO, SPGF44 |
|
|
552
|
|
|
Centromere protein V |
3110013H01Rik, CENP-V, PRR6, p30 |
|
|
553
|
|
|
Cortactin |
EMS1 |
|
|
554
|
|
|
Crystallin beta-gamma domain containing 1 |
AIM1, ST4 |
|
|
555
|
|
|
Cardiomyopathy associated 5 |
C5orf10, SPRYD2, TRIM76 |
|
|
556
|
|
|
Chromosome 7 open reading frame 33 |
- |
|
|
557
|
|
|
C9orf72-SMCR8 complex subunit |
ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1 |
Abulia, Alexia, Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Amyotrophy, Anomia, Anxiety disorder, Aphasia, Apraxia, Arthritis, Behavioral variant of frontotemporal dementia, Brain atrophy, Broca aphasia, Bulbar palsy, Cerebellar ataxia, Cerebral atrophy, Compulsive hoarding, Delusions, Dementia, Dysarthria, Dyscalculia, Dysgraphia, Dyslexia, Dysphagia, Dysphasia, Extrapyramidal dyskinesia, Frontotemporal cerebral atrophy, Frontotemporal dementia, Frontotemporal dementia with motor neuron disease, Grammar-specific speech disorder, Hallucinations, Huntington disease-like, Juvenile arthritis, Laryngospasm, Lateral sclerosis, Mental depression, Mood swings, Nonorganic psychosis, Parkinson disease, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Nonfluent aphasia, Progressive non-fluent aphasia, Psychosis, Ptosis, Respiratory failure, Schizoaffective disorder, Schizophrenia, Seizure, Semantic dementia, Senile plaques, Sensorineural hearing loss, Stereotyped behavior, Still disease, Temporal cortical atrophyView all (40 more) |
|
558
|
|
|
Ceramide synthase 3 |
ARCI9, LASS3 |
Alopecia, Congenital nonbullous ichthyosiform erythroderma, Corneal erosion, Dwarfism, Ectropion, Exfoliative dermatitis, Hypohidrosis, Ichthyosis, Ichthyosis congenita, Ichthyosis with hypotrichosis, Ichthyosis-short stature-brachydactyly-microspherophakia syndrome, Keratitis, Palmoplantar keratoderma, Weill-marchesani syndrome |
|
559
|
|
|
CLN8 transmembrane ER and ERGIC protein |
C8orf61, EPMR, TLCD6 |
Cerebellar atrophy, Cerebral atrophy, Developmental regression, Diabetes mellitus, Disorder of eye, Dyscognitive seizures, Dysmorphic features, Gaucher disease, Leukemia, Mental retardation, Movement disorders, Neuronal ceroid lipofuscinosis, Northern epilepsy syndrome, Progressive epilepsy-intellectual disability syndrome, Psychosis, SeizureView all (1 more) |
|
560
|
|
|
Ciliary associated calcium binding coiled-coil 1 |
ARIEL, C10orf107 |
|
