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1
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Alpha-1-B glycoprotein |
A1B, ABG, GAB, HYST2477 |
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2
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N-acetyltransferase 2 |
AAC2, NAT-2, PNAT |
Acrania, Anencephaly, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Coronary arteriosclerosis, Coronary artery disease, Craniorachischisis, Dermatitis, Diastematomyelia, Industrial dermatosis, Lymphoblastic leukemia, Leukopenia, Liver neoplasms, Liver cancer, Liver carcinoma, Malignant mesothelioma, Marfan syndrome, Neural tube defect, Neurenteric cyst, Primary tethered cord syndrome, Prostatic neoplasms, Prostate cancer, Spinal cord myelodysplasiaView all (11 more) |
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3
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Adenosine deaminase |
ADA1 |
Adenosine deaminase deficiency, Alopecia, Anemia, Asthma, Autism, Autoimmune hemolytic anemia, B-cell lymphoma, Aplasia of the thymus, Dermatitis, Eosinophilia, Exfoliative dermatitis, Hyperemia, Hypothyroidism, Immune thrombocytopenic purpura, Lung neoplasms, Lung cancer, Lymphoma, Mesangial sclerosis, Multiple gastrointestinal atresias, Nephrotic syndrome, Omenn syndrome, Otitis media, Pancreatic adenocarcinoma, Severe combined immunodeficiency disease, Sinusitis, Spinal cord diseases, ThyroiditisView all (12 more) |
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4
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Cadherin 2 |
ACOGS, ADHD8, ARVD14, CD325, CDHN, CDw325, NCAD |
Arrhythmogenic right ventricular cardiomyopathy, Breast cancer, Mammary neoplasms, Breast carcinoma, Developmental delay, Duane retraction syndrome, Gastric cancer, Grand mal status epilepticus, Malformation of cortical development, Marfan syndrome, Mental retardation, Mirror movements, Myocardial ischemia, Nonconvulsive status epilepticus, Petit mal status, Status epilepticus, Stomach neoplasmsView all (2 more) |
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5
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AKT serine/threonine kinase 3 |
MPPH, MPPH2, PKB-GAMMA, PKBG, PRKBG, RAC-PK-gamma, RAC-gamma, STK-2 |
Central nervous system neoplasms, Cortical dysplasia, Cutis marmorata, Developmental delay, Dysmorphic features, Glioblastoma, Glioma, Hemimegalencephaly, Hydrocephalus, Hypoplasia of corpus callosum, Macrocephaly, Malformation of cortical development, Megalanecephaly polymicrogyria-polydactyly hydrocephalus syndrome, Megalencephaly cutis marmorata telangiectatica congenita, Megalencephaly, polymicrogyria, polydactyly, hydrocephalus syndrome, Melanoma, Mental retardation, Microstomia, Polydactyly, Polymicrogyria, Schizophrenia, Strawberry nevus of skin, Postaxial hand polydactyly, Ventricular septal defectView all (9 more) |
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6
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Nuclear receptor subfamily 2 group E member 3 |
ESCS, PNR, RNR, RP37, rd7 |
Cataract, Color blindness, Cone-rod dystrophy, Congenital hypoplasia of penis, Cystoid macular retinal degeneration, Diabetes mellitus, Disorder of eye, Enhanced s-cone syndrome, Glaucoma, Goldmann-favre syndrome, Hearing loss, Hemeralopia, Horizontal nystagmus, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Macular edema, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosa, Retinoschisis, Rod-cone dystrophy, Vitreoretinal degenerationView all (13 more) |
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7
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Small nucleolar RNA, C/D box 116-1 |
HBII-85-1, PWCR1 |
Acromicria, Acromicric dysplasia, Attention deficit hyperactivity disorder, Clinodactyly, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Motor delay, Hypotonia, Penis agenesis, Physiologic amenorrhea, Prader-willi syndrome, Royer syndrome, Scoliosis, Sleep apnea, Somatotropin deficiency, Specific learning disorderView all (7 more) |
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8
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N-acetylated alpha-linked acidic dipeptidase like 1 |
HILAP, I100, NAALADASEL |
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9
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Mitochondrial coiled-coil domain 1 pseudogene 1 |
- |
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10
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ZDHHC20 pseudogene 2 |
- |
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