131
|
|
|
Paired box 2 |
FSGS7, PAPRS, PAX-2 |
Alzheimer disease, Anophthalmia/microphthalmia-esophageal atresia syndrome, Renal hypoplasia, Congenital anomalies of the kidney and urinary tract, Cardiovascular disease, Congenital hypoplasia of kidney, Congenital ocular coloboma, Endometriosis, Idiopathic steroid-resistant nephrotic syndrome, Female infertility, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Gout, Hereditary steroid-resistant nephrotic syndrome, Kidney failure, Metabolic syndrome, Nephrotic syndrome, Nephrotic syndrome, focal segmental type, Optic atrophy, Papillorenal syndrome, Renal cysts and diabetes syndrome, Retinitis pigmentosa, Schizophrenia, Steroid-resistant nephrotic syndrome, Diabetes mellitus type 2, Uterine prolapseView all (12 more) |
132
|
|
|
Paired box 3 |
CDHS, HUP2, PAX-3, WS1, WS3 |
Alzheimer disease, Androgenetic alopecia, Asthma, Central precocious puberty, Congenital diaphragmatic hernia, Congenital hand deformities, Congenital neurologic anomalies, Craniofacial abnormalities, Craniofacial deafness hand syndrome, Deafness, Desbuquois syndrome, Hearing impairment, Insomnia, Intellectual developmental disorder, Kleins syndrome, Neural tube defect, Neural tube defects, x-linked, Rhabdomyosarcoma, Sarcoma, Scoliosis, Usher syndrome, Waardenburg syndromeView all (7 more) |
133
|
|
|
Paired box 4 |
KPD, MODY9 |
Attention deficit hyperactivity disorder, Autism, Kidney disease, Diabetes mellitus, Diabetes mellitus type 1, Diabetes mellitus ketosis prone, Diabetes mellitus type 2, Diabetic eye disease, Diabetic ketoacidosis, Diabetic retinopathy, Duodenal ulcer, Gestational diabetes, Hyperglycemia, Kidney failure, Maturity-onset diabetes of the young (mody), Melanoma, Maturity-onset diabetes of the youngView all (2 more) |
134
|
|
|
Paired box 5 |
ALL3, BSAP, PAX-5 |
Anxiety disorder, Bipolar disorder, B-lymphoblastic leukemia/lymphoma, Breast cancer, Coronary artery disease, Estrogen-receptor negative breast cancer, Iga nephropathy, Insomnia, Lymphoblastic leukemia, Major depressive disorder, Metabolic syndrome, Neurodevelopmental disorder, Neurotic disorder, Obesity, Schizophrenia, Stroke, Diabetes mellitus type 2View all (2 more) |
135
|
|
|
Paired box 6 |
AN, AN1, AN2, ASGD5, D11S812E, FVH1, MGDA, WAGR |
Aniridia, Aniridia-cerebellar ataxia-intellectual disability syndrome, Anophthalmia/microphthalmia-esophageal atresia syndrome, Anophthalmia, Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Autism, Keratitis, Axenfeld-rieger syndrome, Cataract, Congenital cataract, Cataract-corneal dystrophy syndrome, Paranoid schizophrenia, Cleft eyelid, Coloboma, Commissural facial cleft, Congenital aniridia, Congenital iris coloboma, Congenital neurologic anomalies, Congenital nystagmus, Congenital ocular coloboma, Craniofacial abnormalities, Developmental disability, Diabetes mellitus, Diabetes mellitus type 2, Optic nerve disorder, Gillespie syndrome, Insomnia, Intellectual developmental disorder, Major depressive disorder, Melanoma, Microphthalmia, Microphthalmos, Neurotic disorder, Nystagmus, Schizophrenia, Prostatic neoplasms, Retinitis pigmentosa, Stomach neoplasms, Tooth abnormalities, Wagr syndrome, Wilms tumorView all (27 more) |
136
|
|
|
Paired box 7 |
CMYO19, CMYP19, HUP1, MYOSCO, PAX7B, RMS2 |
Color vision deficiency, Congenital myopathy, Gestational diabetes, Kidney disease, Lung cancer, Lymphedema, Malignant glioma, Orofacial cleft, Osteoarthritis, Parkinson disease, Psoriasis, Rhabdomyosarcoma |
137
|
|
|
Paired box 8 |
PAX-8 |
Congenital hypothyroidism, Breast cancer, Cancer, Cervical cancer, Cervical intraepithelial neoplasia, Colorectal cancer, Colorectal neoplasms, Thyroid agenesis, Congenital thyroid atrophy, Congenital hypothyroidism due to absence of thyroid gland, Congenital hypothyroidism without goiter, Differentiated thyroid carcinoma, Dry eye syndrome, Estrogen-receptor negative breast cancer, Gout, Insomnia, Lung cancer, Ovarian cancer, Ovarian mucinous adenocarcinoma, Ovarian serous carcinoma, Prostate cancer, Spermatocele, Squamous cell carcinoma, Testicular disease, Testicular hydrocele, Follicular thyroid cancerView all (11 more) |
138
|
|
|
Paired box 9 |
STHAG3 |
|
139
|
|
|
PAX3 and PAX7 binding protein 1 |
BM020, C21orf66, FSAP105, GCFC, GCFC1 |
|
140
|
|
|
PAX interacting protein 1 |
CAGF28, CAGF29, PACIP1, PAXIP1L, PTIP, TNRC2 |
|
