101
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|
|
ATP binding cassette subfamily C member 9 |
ABC37, ATFB12, CANTU, CMD1O, IDMYS, SUR2 |
Curated: Acromegaloid facial appearance syndrome, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Brugada syndrome, Cantu syndrome, Cardiomyopathy, Dilated cardiomyopathy, Congenital epicanthus, Desbuquois syndrome, Endometrial neoplasms, Endometriosis, Epilepsy, Gout, Hereditary atrial fibrillation, Hypertrichosis, Hypertrophic cardiomyopathy, Intellectual disability and myopathy syndrome, Kleefstra syndrome, Left ventricular disease, Micrognathism, Obesity, Patent ductus arteriosus, Pelvic organ prolapse, Scoliosis, Depression, Wolff-parkinson-white syndrome, hypertrichotic osteochondrodysplasia Cantu type, dilated cardiomyopathy 1O
Unreviewed: Alzheimer disease, Amyotrophic Lateral Sclerosis, Asthma, Atrial Fibrillation, Atrioventricular block, Atrophy, Bicuspid aortic valve, Blepharophimosis, Bohring syndrome, Brain atrophy, Brain disease, Brugada Syndrome, Bundle Branch Block, Cardiac arrhythmias, Cardiomegaly, Cardiovascular Abnormalities, Cardiovascular Diseases, Central core myopathy, Cerebral Atrophy, Cerebral palsy, Chronic obstructive pulmonary disease, Congenital Epicanthus, Congenital Exomphalos, Congestive Heart Failure, Coronary Artery Vasospasm, Deafness, Dilated Cardiomyopathy, Dysmorphic Features, Endometrial carcinoma, Endometrial neoplasm, Endometrial Neoplasms, Endometrioma, Facial dysmorphism syndrome, Gouty arthritis, Hearing Loss, Heart disease, Heart Diseases, Heart Failure, Hepatocellular carcinoma, Hirschsprung disease, Hypertension, HYPERTRICHOSIS, Hypertrichosis-Acromegaloid Facial Appearance Syndrome, Hypertrichotic osteochondrodysplasia, Impaired myocardial contractility, Lipoatrophy, Lipodystrophy, Long QT Syndrome, Lung neoplasms, Lymphedema, Macrocephaly, Macroglossia, Macrostomia, Mental Depression, Mental retardation, Migraine, Multiple Congenital Anomalies, Myocardial Infarction, Myopathy, Narcolepsy, Osteochondrodysplasia, Osteoporosis, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Paroxysmal ventricular tachycardia, Pericardial effusion, Prostatic neoplasm, Pseudoxanthoma elasticum, Short qt syndrome, Sick Sinus Syndrome, Skeletal Dysplasia, Spherocytosis, Stomach neoplasms, Supraventricular tachycardia, Syndactyly of fingers, Synophrys, Trifascicular block, Ventricular arrhythmia, Ventricular Congenital Hypertrophy, Ventricular Fibrillation, Ventricular tachycardia, Wolff-Parkinson-White Syndrome
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102
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|
|
ATP binding cassette subfamily D member 1 |
ABC42, ALD, ALDP, AMN |
Curated: Adrenoleukodystrophy, Bipolar disorder, Congenital neurologic anomalies, Deafness, dystonia, and cerebral hypomyelination, Ehlers-danlos syndrome, Encephalitis, Hirschsprung disease, Intellectual developmental disorder, Major depressive disorder, Peroxisome biogenesis disorder, Schizophrenia, Spastic paraplegia, Hereditary spastic paraplegia, Spondyloepimetaphyseal dysplasia, X-linked cerebral adrenoleukodystrophy
Unreviewed: Addison`s Disease, Adrenal Cortical Hypofunction, Adrenomyeloneuropathy, Agenesis Of Corpus Callosum, Alopecia, Asthma, Atherosclerosis, Attention Deficit Hyperactivity Disorder, Autoimmune Diseases, Autoimmune Lymphoproliferative Disorder, Bowel incontinence, Brain disease, Bulbar palsy, Carcinogenesis, Carpal Tunnel Syndrome, Cerebral Adrenoleukodystrophy, X-Linked, Cerebral Infraction, Cerebral palsy, Cerebrovascular disorder, Cerebrovascular Disorders, Cholestasis, Cirrhosis, Congenital Microcephaly, Contiguous ABCD1 DXS1357E Deletion Syndrome, Dementia, Dementia Of Frontal Lobe, Demyelinating Diseases, Developmental Delay, Developmental regression, Diabetes mellitus, type 2, End Stage Liver Disease, Endocrine System Diseases, Epilepsy, Erectile Dysfunction, Fatty Liver, Glomerulonephritis, Hearing Loss, Heart disease, Huntington Disease, Hyperaldosteronism, Hypoadrenocorticism, Hypogonadism, Immune System Diseases, Ischemic Stroke, Kidney neoplasm, Language Disorders, Leukodystrophy, Leukoencephalopathy, Liver carcinoma, Liver Cirrhosis, Lung Neoplasms, Lupus Erythematosus, Lupus Nephritis, Lupus Vulgaris, Lymphoproliferative Disorder, Malignant Neoplasm, Melanoma, Metabolic Diseases, Metabolic syndrome, Metachromatic leukodystrophy, Movement disorder, Myocarditis, Neoplasms, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neurodegenerative Disorders, Non-Alcoholic Fatty Liver Disease, Pancreatic Diseases, Peripheral Neuropathy, Peroxisomal disorder, Polyneuropathy, Psychosis, Renal Carcinoma, Renal cell carcinoma, Sclerosing Cholangitis, Scoliosis, Senile Dementia, Spastic tetraparesis, Spinal cord compression, Spinal Cord Diseases, Spinal muscular atrophy, Spinocerebellar Ataxia, Spondyloarthritis, Squamous cell carcinoma, Tangier Disease, Thoracolumbar scoliosis, Visual disorder, Zellweger Syndrome
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103
|
|
|
ATP binding cassette subfamily D member 1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
104
|
|
|
ATP binding cassette subfamily D member 1 pseudogene 2 |
bA453N3.6 |
Curated: N/A
Unreviewed: N/A
|
105
|
|
|
ATP binding cassette subfamily D member 1 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
106
|
|
|
ATP binding cassette subfamily D member 1 pseudogene 4 |
ALD22Q11 |
Curated: N/A
Unreviewed: N/A
|
107
|
|
|
ATP binding cassette subfamily D member 1 pseudogene 5 |
- |
Curated: N/A
Unreviewed: N/A
|
108
|
|
|
ATP binding cassette subfamily D member 2 |
ABC39, ALDL1, ALDR, ALDRP, hALDR |
Curated: Alzheimer disease, Colorectal neoplasms
Unreviewed: Acne, Adrenoleukodystrophy, Adrenomyeloneuropathy, Arthritis, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cerebral Infarction, Cerebral Ischemia, Colorectal Cancer, Colorectal Neoplasms, Diabetes, Diabetes Mellitus, Hepatocellular carcinoma, Hypercholesterolemia, Ischemic Stroke, Liver carcinoma, Neurodegenerative Disorders, Ovarian neoplasm, Pancreatic adenocarcinoma, Prostatic neoplasm, Pseudoxanthoma elasticum, Speech Disorders, Stroke, Transient Ischemic Attack, Zellweger Syndrome
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109
|
|
|
ATP binding cassette subfamily D member 3 |
ABC43, CBAS5, PMP70, PXMP1, ZWS2 |
Curated: Congenital bile acid synthesis defect, Colorectal neoplasms, Oculopharyngodistal myopathy
Unreviewed: Adrenoleukodystrophy, Adrenomyeloneuropathy, Carcinoma, Cerebral Ischemia, Colorectal Cancer, Colorectal Neoplasms, Congenital Bile Acid Synthesis Defect, Glioma, Hepatocellular carcinoma, Iron deficiency anemia, Liver failure, Liver Fibrosis, Lymphoma, Prostatic neoplasm, Stroke, Sveinsson chorioretinal atrophy, Transient Ischemic Attack, Zellweger Syndrome, Zellweger-Like Syndrome
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110
|
|
|
ATP binding cassette subfamily D member 4 |
ABC41, EST352188, MAHCJ, P70R, P79R, PMP69, PXMP1L |
Curated: Cobalamin c disease, Colorectal neoplasms, Intracellular cobalamin metabolism disorder, Methylmalonic acidemia, Ocular sarcoidosis, Vitamin b deficiency, methylmalonic acidemia with homocystinuria, type cblJ
Unreviewed: Adrenoleukodystrophy, Adrenomyeloneuropathy, Anemia, Cobalamin deficiency, Colorectal Cancer, Colorectal Neoplasms, Fatigue syndrome, Homocystinuria, Inborn Errors Of Metabolism, Methylmalonic acidemia with homocystinuria, Neutropenia
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