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751
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CD46 molecule |
AHUS2, MCP, MIC10, TLX, TRA2.10 |
C3 glomerulopathy, Colorectal cancer, Complement component deficiency, Disseminated intravascular coagulation, Eclampsia, Febrile seizures, Fibrinogen deficiency, Hellp syndrome, Hemolytic uremic syndrome, Hypertension, Hypofibrinogenemia, Maternal hypertension, Microangiopathic hemolytic anemia, Pleural effusion, Prostatic cancer, castration-resistant, Prostatic neoplasms, castration-resistantView all (1 more) |
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752
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Class II major histocompatibility complex transactivator |
C2TA, CIITAIV, MHC2D1, MHC2TA, NLRA |
Addison`s disease, Agammaglobulinemia, Autoimmune hemolytic anemia, Bare lymphocyte syndrome, Celiac disease, Cholangitis, Colitis, Digestive system neuroendocrine neoplasm, Drachtman weinblatt sitarz syndrome, Dysarthria, Encephalitis, Immune thrombocytopenic purpura, Malabsorption syndrome, Nasopharyngeal neoplasms, Neutropenia, Otitis media, Pancytopenia, Rheumatoid arthritis, Rhinitis, Sinusitis, VasculitisView all (6 more) |
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753
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CD99 molecule (Xg blood group) |
HBA71, MIC2, MIC2X, MIC2Y, MSK5X |
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|
754
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|
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C-X-C motif chemokine ligand 9 |
CMK, Humig, MIG, SCYB9, crg-10 |
Alopecia areata, Biliary cirrhosis, Breast cancer, Mammary neoplasms, Breast carcinoma, Carotid artery stenosis, Celiac disease, Common carotid artery stenosis, Endometrioma, Endometriosis, External carotid artery stenosis, Internal carotid artery stenosis, Interstitial cystitis, Malignant mesothelioma, Marfan syndrome, Biliary cholangitisView all (1 more) |
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755
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Coiled-coil and HOOK domain protein 88C |
DAPLE, HKRP2, HYC1, KIAA1509, SCA40 |
Aqueductal stenosis, Spinocerebellar ataxia, Breast cancer, Breast carcinoma, Communicating hydrocephalus, Congenital hydrocephalus, Congenital non-communicating hydrocephalus, Dysarthria, Fetal cerebral ventriculomegaly, Hydrocephalus, Hydrocephalus ex-vacuo, Mental retardation, Obstructive hydrocephalus, Schizophrenia, Supranuclear gaze palsy |
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756
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CATSPER2 pseudogene 1 |
CATSPER2B |
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757
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Calpain 14 |
- |
|
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758
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|
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Mitochondrially encoded cytochrome c oxidase I |
COI, MTCO1 |
Addison`s disease, Anaplastic carcinoma, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Carcinoma, Cardiomyopathy, Cataract, Central visual impairment, Cerebral cortical atrophy, Colorectal cancer, Congestive heart failure, Cytochrome-c oxidase deficiency, Deafness, nonsyndromic sensorineural, mitochondrial, Dementia, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Left ventricular hypertrophy, Malabsorption syndrome, Malformation of cortical development, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial myopathy, Multiple lipomata, Myocardial diseases, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Optic atrophy, Palmoplantar keratoderma with deafness, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Tetralogy of fallot, Thyroiditis, Ventricular preexcitationView all (54 more) |
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759
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Mitochondrially encoded cytochrome c oxidase II |
COII, MTCO2 |
Addison`s disease, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cataract, Central visual impairment, Cerebral cortical atrophy, Colorectal cancer, Congestive heart failure, Cytochrome-c oxidase deficiency, Dementia, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Left ventricular hypertrophy, Malabsorption syndrome, Malformation of cortical development, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial diseases, Mitochondrial myopathy, Multiple lipomata, Myopathy, Nephrotic syndrome, Neuroblastoma, Nyctalopia, Optic atrophy, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Seizure, Sensorineural hearing loss, Tetralogy of fallot, Thyroiditis, Wolff-parkinson-white syndromeView all (46 more) |
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760
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|
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Mitochondrially encoded cytochrome c oxidase III |
COIII, MTCO3 |
Addison`s disease, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Cytochrome-c oxidase deficiency, Dementia, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Epilepsy, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Left ventricular hypertrophy, Leigh syndrome, Malabsorption syndrome, Malformation of cortical development, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial encephalopathy, Mitochondrial myopathy, Multiple lipomata, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Optic atrophy, Pancreatitis, Polyneuropathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Tetralogy of fallot, Thyroiditis, Ventricular preexcitationView all (51 more) |
