331
|
|
|
NDRG family member 4 |
BDM1, SMAP-8, SMAP8 |
Curated: Achromatopsia, Autism, Schizophrenia
Unreviewed: Adenoma, Adrenocortical carcinoma, Agenesis Of Corpus Callosum, Aplasia Cutis Congenita, Carcinogenesis, Cerebral Infarction, Colitis, Colorectal Cancer, Colorectal neoplasm, Epilepsy, Glioblastoma, Glioma, Hyperplasia, Inflammatory Bowel Disease, Intestinal disease, Long qt syndrome, Malignant Neoplasm, Meningioma, Miscarriage, Mouth neoplasm, Myofibromatosis, Neoplasms, Obesity, Pancreatic ductal carcinoma, Pancreatic neoplasm, Promyelocytic leukemia, Prostate cancer, Stomach Carcinoma, Stomach Neoplasms, Tetralogy of fallot, Ulcerative colitis
|
332
|
|
|
N-deacetylase and N-sulfotransferase 1 |
HSST, MRT46, NST1 |
Curated: Nonsyndromic intellectual disability, Cleft lip and palate, Craniofacial abnormalities, Eye abnormalities, Gastrointestinal stromal tumor, Global developmental delay, Intellectual developmental disorder, Cortical development malformation, Osteoarthritis
Unreviewed: Absence Of Septum Pellucidum, Autism, Breast Cancer, Breast Carcinoma, Breast neoplasm, Central Visual Impairment, Cerebral Atrophy, Cirrhosis, Congenital alveolar dysplasia, Congenital diaphragmatic hernia, Cortical Dysplasia, Developmental Delay, Diabetes, Diabetes Mellitus, Dyskinetic Syndrome, Dyssomnia, Eosinophilia, Glioblastoma, Glioma, Holoprosencephaly, Hypoplasia Of Corpus Callosum, Kidney Disease, Liver Cirrhosis, Malformation of cortical development, Malignant Neoplasm, Mandibulofacial Dysostosis, Meningioma, Mental Depression, Mental retardation, Microcephaly, Motor delay, Myocardial Infarction, Neoplasms, Nephrosis, Non-Syndromic Intellectual Disability, Polymicrogyria, Pulmonary hypoplasia, Renal Carcinoma, Respiratory Failure, Rheumatoid arthritis, Salaam Seizures, Seizure, Sleep Disorders, Stereotyped Behavior
|
333
|
|
|
NDST1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
334
|
|
|
N-deacetylase and N-sulfotransferase 2 |
HSST2, N-HSST 2, NST2 |
Curated: Myocardial infarction, Prostatic neoplasms, Schizophrenia
Unreviewed: Glioma, Hypoxia, Meningioma, Prostate cancer, Prostatic Neoplasms
|
335
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
336
|
|
|
N-deacetylase and N-sulfotransferase 3 |
HSST3 |
Curated: Bipolar disorder, Kidney disease, Keratoconus, Metabolic syndrome, Neurotic disorder, Willis-ekbom disease, Schizophrenia, Diabetes mellitus type 2
Unreviewed: Alzheimer disease, Amyotrophic lateral sclerosis, Anxiety Disorder, Bipolar Disorder, Colorectal Cancer, Frontotemporal dementia, Glioma, Liver neoplasm, Mental Depression, Mental Disorders, Narcolepsy, Parkinson disease, Renal cell carcinoma
|
337
|
|
|
N-deacetylase and N-sulfotransferase 4 |
N-HSST, N-HSST 4, NDST-4, NHSST4 |
Curated: Alzheimer disease, Liver cirrhosis, Dementia, Osteoarthritis, Prostatic neoplasms, Willis-ekbom disease
Unreviewed: Bipolar disorder, Bladder exstrophy, Colorectal Cancer, Colorectal neoplasm, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Diabetes mellitus, type 2, Language development disorders, Language Disorders, Malignant Neoplasm, Neoplasms, Prostate cancer, Prostatic Neoplasms
|
338
|
|
|
NADH:ubiquinone oxidoreductase subunit A1 |
CI-MWFE, MC1DN12, MWFE, ZNF183 |
Curated: Leigh syndrome, Mitochondrial complex deficiency, mitochondrial disease
Unreviewed: Alzheimer disease, Carcinoma, Choreoathetosis, Cognition disorder, Colorectal Cancer, Dementia, Developmental Delay, Diabetes Mellitus, Epileptic encephalopathy, Glioma, Hearing Loss, Hereditary Leber Optic Atrophy, Huntington Disease, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leigh Syndrome, Leukodystrophy, Leukoencephalopathy, MELAS Syndrome, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Myoclonic Epilepsy, Myoclonic Seizures, Necrotizing encephalomyelopathy, Neurodegenerative disorder, Neurodegenerative Disorders, Nystagmus, Optic Neuropathy, Oxidative Phosphorylation Deficiency, Parkinson disease, Ptosis, Strabismus
|
339
|
|
|
NADH:ubiquinone oxidoreductase subunit A10 |
CI-42KD, CI-42k, MC1DN22 |
Curated: Alzheimer disease, Appendicitis, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Essential tremor, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Schizophrenia
Unreviewed: Anemia, Cerebellar Ataxia, Dementia, Developmental Delay, Diabetes mellitus, type 2, Dysarthria, Hypertension, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Leigh Syndrome, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Mental retardation, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mood swings, Necrotizing encephalomyelopathy, Nervous System Diseases, Nystagmus, Optic Atrophy, Prostatic neoplasm, Ptosis, Retinitis Pigmentosa, Strabismus, Ventricular septal defect
|
340
|
|
|
NADH:ubiquinone oxidoreductase subunit A11 |
B14.7, CI-B14.7, MC1DN14 |
Curated: Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Amyloidosis, Brain atrophy, Cerebral Atrophy, Developmental Delay, Diabetes Mellitus, Epileptic encephalopathy, Hearing Loss, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leukodystrophy, Leukoencephalopathy, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial myopathy, Myopathy, Nystagmus, Optic Atrophy, Ptosis, Strabismus
|