111
|
|
|
PAGE family member 3 |
CT16.6, GAGED1, PAGE-3 |
Curated: Androgenetic alopecia, Neurotic disorder
Unreviewed: N/A
|
112
|
|
|
PAGE family member 4 |
CT16.7, GAGE-9, GAGEC1, JM-27, JM27, PAGE-1, PAGE-4 |
Curated: Prostate cancer
Unreviewed: Benign Prostatic Hyperplasia, Colorectal Cancer, Congenital Arteriovenous Malformation, Head and neck neoplasm, Malignant Neoplasm, Prostatic disease, Prostatic hyperplasia, Prostatic neoplasm, Stomach Neoplasms, Tumor
|
113
|
|
|
PAGE4 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
114
|
|
|
PAGE family member 5 |
CT16, CT16.1, CT16.2, GAGEE1, PAGE-5 |
Curated: N/A
Unreviewed: Head and neck neoplasm, Lung carcinoma, Malignant Neoplasm, Melanoma, Neoplasms
|
115
|
|
|
PAXIP1 associated glutamate rich protein 1 |
C16orf53, GAS, PA1 |
Curated: Neurodevelopmental disorder
Unreviewed: Acne, Adenocarcinoma, Age-related macular degeneration, Alpha thalassemia, Amyloidosis, Anxiety Disorder, Astrocytoma, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiovascular Diseases, Cholangiocarcinoma, Chronic Obstructive Pulmonary Disease, Cognition disorder, Diabetes, Diabetes Mellitus, Fabry disease, Glioma, Glomerulonephritis, Heart Diseases, Heart failure, Hepatolenticular Degeneration, Hypertrophy Of Tonsils, Idiopathic pulmonary fibrosis, Lung carcinoma, Lung disease, Lung neoplasms, Lymphocytic Leukemia, Malignant Neoplasm, Mental Disorders, Multiple system atrophy, Myocardial Infarction, Myositis, Osteochondrodysplasias, Ovarian neoplasm, Parkinson disease, Pharyngitis, Prostate cancer, Prostatic neoplasm, Pseudohypoparathyroidism, Pyoderma, Rheumatic Heart Disease, Septicemia, Sickle cell anemia, Stomach Carcinoma, Stomach Neoplasms, Thyroid hormone resistance, Uterine neoplasm
|
116
|
|
|
Phenylalanine hydroxylase |
PH, PKU, PKU1 |
Curated: Atypical femoral fracture, Autism, Hyperphenylalaninemia, Biliary atresia, Haddad syndrome, Phenylketonuria, Congenital central hypoventilation syndrome, Intellectual developmental disorder, Neurodevelopmental disorder, Pituitary dwarfism, Psychotic disorders, Pulmonary hypertension, Schizophrenia, Tetrahydrobiopterin-responsive phenylketonuria
Unreviewed: 6-pyruvoyl-tetrahydropterin synthase deficiency, Amyotrophic Lateral Sclerosis, Anxiety Disorder, Aortic Coarctation, Arteriosclerosis, Arthritis, Ataxia Telangiectasia, Atherosclerosis, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Bipolar Disorder, Bladder Exstrophy, Bone marrow failure syndromes, Brachydactyly, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bruton type agammaglobulinemia, Carcinoma, Cardiomyopathy, Cardiovascular Diseases, Cataract, Chronic disease, Chronic Obstructive Pulmonary Disease, Clinodactyly, Complement component deficiency, Congenital Central Hypoventilation, Congenital Epicanthus, Congenital heart defects, Congenital Heart Disease, Connective Tissue Disease, Coronary artery disease, CREST Syndrome, Cystic Fibrosis, Cystinuria, Deficiency Of Glucose-6-Phosphate Dehydrogenase, Delusions, Developmental Delay, Disorder of amino acid metabolism, Double Outlet Right Ventricle, Down Syndrome, Duchenne Muscular Dystrophy, Eczema, Emphysema, Esophageal Atresia, Esophageal Carcinoma, Esophagus Neoplasm, Galactosemia, Glaucoma, Glioma, Hallucinations, Heart Diseases, Heart Failure, HELLP Syndrome, Hematologic neoplasm, Hepatolenticular Degeneration, High palate, Hyperinsulinism, Hypersensitivity, Hypertension, Hypoglycemia, Hypopigmentation Disorder, Hypoplasia Of Corpus Callosum, Hypoplastic Left Heart Syndrome, Inborn Errors Of Metabolism, Keratosis Follicularis, Kidney Disease, Leiomyoma, Leukemia, Lung Cancer, Lung carcinoma, Lung disease, Lung Diseases, Lupus Erythematosus, Machado-Joseph Disease, Malignant Neoplasm, Malnutrition, Maple Syrup Urine Disease, Maternal Phenylketonuria, Melanoma, Mental Depression, Mental Disorders, Mental retardation, Metabolic Diseases, Metachromatic leukodystrophy, Microcephaly, Micrognathism, Mitochondrial disease, Myelodysplastic syndrome, Myeloid leukemia, Neoplasms, Neuroblastoma, Obsessive-Compulsive Disorder, Osteopenia, Osteoporosis, Paraplegia, Parkinson disease, Pericardial effusion, Polycythemia vera, Psychosis, Pulmonary arterial hypertension, Pulmonary Arterial Hypertension Associated With Congenital Heart Disease, Pulmonary Arterial Hypertension Associated With Connective Tissue Disease, Pulmonary Hypertension, Pulmonary venoocclusive disease, Scleroderma, Spinocerebellar Ataxia, Strabismus, Systemic sclerosis, Tetralogy of Fallot, Thrombocytopenia, Transient hyperphenylalaninemia, Tricuspid atresia, Triple negative breast cancer, Tuberous Sclerosis, Vascular Diseases, Ventricular septal defect, Vitiligo, Vitiligo-associated SYSTEMIC LUPUS ERYTHEMATOSUS, Xeroderma Pigmentosum
|
117
|
|
|
Phosphoribosylaminoimidazole carboxylase and phosphoribosylaminoimidazolesuccinocarboxamide synthase |
ADE2, ADE2H1, AIRC, PAICSD, PAIS |
Curated: Phosphoribosylaminoimidazole carboxylase deficiency, Schizophrenia
Unreviewed: 46, XY disorder of sex development, 5-alpha reductase deficiency, Androgen-Insensitivity Syndrome, Atrophy, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Colorectal Cancer, Colorectal neoplasm, Cryptorchidism, Developmental disability, Glioblastoma, Glioma, Glycogen storage disease, Gonadal Dysgenesis, Malignant Neoplasm, Melanoma, Neoplasms, Neuroblastoma, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Psychiatric disorders, Reifenstein Syndrome, Sex Differentiation Disorders, Squamous cell carcinoma, Stroke, Testicular Feminization, Turner Syndrome
|
118
|
|
|
Phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
119
|
|
|
Phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
120
|
|
|
Phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|