1121
|
|
|
OSTN antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Triple Negative Breast Neoplasms
|
1122
|
|
|
Ornithine transcarbamylase |
OCTD, OTC1, OTCD, OTCase |
Curated: Brain disease, Cognition disorder, Delirium, dementia, and cognitive disorders, Urea cycle disorder, Global developmental delay, Hyperammonemia, ornithine carbamoyltransferase deficiency
Unreviewed: Adrenal Hypoplasia, X-Linked, Androgenetic Alopecia, Argininosuccinic aciduria, Brain Neoplasms, Carbamoyl Phosphate Synthase Deficiency, Central nervous system disease, Cirrhosis, Citrullinemia, Cognitive disorder, Colorectal Cancer, Colorectal neoplasm, Comedone, Congenital adrenal hypoplasia, Congenital Chromosomal Disease, Congenital disorder of glycosylation, Congenital stationary night blindness, X-Linked, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Developmental Delay, Duchenne And Becker Muscular Dystrophy, Duchenne Muscular Dystrophy, Edema, Epileptic encephalopathy, Episodic Ataxia, Fatty Liver, Galactosemia, Gonadotropin Deficiency, Granulomatous Disease, Hepatoblastoma, Hepatocellular carcinoma, Hereditary orotic aciduria, HMG CoA Lyase Deficiency, Hydrocephalus Syndrome, X-Linked, Hypersensitivity, Hypertension, Hypoglycemia, Hypogonadism, Inborn Errors Of Metabolism, Liver carcinoma, Liver Cirrhosis, Liver disease, Liver failure, Liver Fibrosis, Lung carcinoma, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Malnutrition, Maple syrup urine disease, Mental retardation, Metabolic Diseases, Metabolic syndrome, Migraine, Mitochondrial Diseases, Mood disorder, Myelomonocytic Leukemia, Myopia, Neoplasms, Niemann-Pick Disease, Night blindness, Nyctalopia, Ocular albinism, Ornithine Carbamoyltransferase Deficiency, Ornithine Transcarbamylase Deficiency, Pancreatitis, Periodontal Diseases, Pharyngitis, Phenylketonuria, Properdin Deficiency, Prostatic neoplasm, Retinitis Pigmentosa, Retinitis Pigmentosa, X-Linked, Severe combined immunodeficiency disease, Syndromic microphthalmia, Trichohepatoenteric Syndrome, Tyrosinemia, Vitamin d deficiency, Wiskott-Aldrich Syndrome
|
1123
|
|
|
- |
C11DELq13, DEL11q13 |
Curated: N/A
Unreviewed: N/A
|
1124
|
|
|
Otoancorin |
CT108, DFNB22 |
Curated: Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing loss, Hereditary hearing loss, Major depressive disorder, Schizophrenia, Usher syndrome, nonsyndromic genetic hearing loss
Unreviewed: Adrenogenital Syndrome, Alpha 1-Antitrypsin Deficiency, Complement Component Deficiency, Congenital adrenal hyperplasia, Cytochrome-C Oxidase Deficiency, Hearing Loss, Myeloid leukemia, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Osteoarthritis, Von Willebrand Disorder
|
1125
|
|
|
OTOA pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1126
|
|
|
Otoferlin |
AUNB1, DFNB6, DFNB9, FER1L2, NSRD9 |
Curated: Alzheimer disease, Arthrogryposis with ectodermal dysplasia, Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic intellectual disability, Congenital ear anomaly, Deafness, Hearing loss, Hereditary hearing loss, Pendred syndrome, Periodontitis, Nonsyndromic hearing loss, nonsyndromic genetic hearing loss
Unreviewed: Absence epilepsy, Auditory Neuropathy, Breast Cancer, Breast neoplasm, Cochlear diseases, Corneal dystrophy, Dermatomyositis, Headache, Hearing Impairment, Hearing Loss, Language development disorders, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Sensorineural hearing loss, Tourette syndrome, Usher Syndrome
|
1127
|
|
|
Otogelin |
DFNB18B, MLEMP, OTGN |
Curated: Amyotrophic lateral sclerosis, Asthma, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing loss, Intellectual developmental disorder, Meniere disease, nonsyndromic genetic hearing loss
Unreviewed: Conductive hearing loss, Developmental dysplasia of the hip, Lateral Sclerosis, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Vestibular disease
|
1128
|
|
|
Otogelin like |
C12orf64, DFNB84B |
Curated: Alzheimer disease, Isolated sensorineural deafness, Nonsyndromic intellectual disability, Central vertigo, Kidney disease, Deafness, Hearing loss, Meniere disease, Ocular hypertension, Oligodendroglioma, Peripheral vertigo, Nonsyndromic hearing loss, Skin disease, Vestibular disease, nonsyndromic genetic hearing loss
Unreviewed: Breast Cancer, Conductive hearing loss, Hearing Loss, Kidney Disease, Kidney Failure, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness
|
1129
|
|
|
Otolin 1 |
C1QTNF15, C1QTNF16 |
Curated: Alzheimer disease, Attention deficit hyperactivity disorder, Burkitt lymphoma, Coronary artery disease, Dementia, Eosinophilia, Eyelid disease, Glomerulonephritis, Kidney disease, Lung cancer, Major depressive disorder, Metabolic syndrome, Oligodendroglioma, Schizophrenia, Squamous cell carcinoma, Diabetes mellitus type 2
Unreviewed: Meniere disease
|
1130
|
|
|
Otopetrin 1 |
- |
Curated: N/A
Unreviewed: N/A
|