|
341
|
|
|
Paired box 6 |
AN, AN1, AN2, ASGD5, D11S812E, FVH1, MGDA, WAGR |
11p deletion syndrome, Ambiguous genitalia, Anencephaly, Aniridia, Aniridia, cerebellar ataxia, and mental retardation, Anomalous pulmonary artery, Anterior pituitary dysgenesis, Anterior segment dysgenesis, Anxiety disorder, Autism, Axenfeld anomaly, Cataract, Congenital cataract with corneal dystrophy, Coloboma of eye, Coloboma of macula, Coloboma of optic disc, Congenital cataract, Congenital coloboma of iris, Congenital nystagmus, Congenital ocular coloboma, Contiguous gene syndrome, Cryptorchidism, Developmental delay, Diabetes, Diabetes mellitus, Disorder of eye, Drachtman weinblatt sitarz syndrome, Dwarfism, Foster-kennedy syndrome, Foveal hypoplasia, Foveal hypoplasia-presenile cataract syndrome, Fundus coloboma, Gastric cancer, Gillespie syndrome, Glaucoma, Glaucoma, congenital, Hypoplasia of corpus callosum, Hypoplasia of optic disc, Hypoplasia of the optic nerve, Hypospadias, Mental retardation, Keratitis, Keratitis, hereditary, Lens coloboma, Melanoma, Microcephaly, Micrognathism, Microphthalmia with coloboma, Microphthalmos, Morning glory anomaly, Morning glory syndrome, Movement disorders, Nephroblastoma, Nystagmus, Obesity, Odontome, Optic atrophy, Optic disc disorder, Optic nerve aplasia, Optic nerve hypoplasia, O`donnell pappas syndrome, Persistent hyperplastic primary vitreous, Polymicrogyria, Presenile cataract, Prostatic neoplasms, Prostate cancer, Pseudopapilledema, Ptosis, Retinal coloboma, Retinal detachment, Schizophrenia, Scoliosis, Stomach neoplasms, Strabismus, Streak ovary, Subcapsular cataract, Syndromic microphthalmia, Synechiae, Uranostaphyloschisis, Uveoretinal coloboma, Vesicoureteral reflux, Wagner syndrome, Wagr syndromeView all (68 more) |
|
342
|
|
|
Paired box 7 |
CMYO19, CMYP19, HUP1, MYOSCO, PAX7B, RMS2 |
|
|
343
|
|
|
Paired box 9 |
STHAG3 |
Breast cancer, Breast carcinoma, Hypodontia, Hypoplasia of the maxilla, Microdontia, Micrognathism, Oligodontia, Prostate cancer, Prostate cancer, hereditary, Tooth agenesis |
|
344
|
|
|
PBX homeobox 1 |
CAKUHED |
African burkitt`s lymphoma, Ambiguous genitalia, Bilateral renal hypoplasia, Burkitt`s lymphoma, Congenital anomalies of kidney and urinary tract, Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay, Congenital diaphragmatic hernia, Congenital epicanthus, Cryptorchidism, Ectopic kidney, Horseshoe kidney, Leukemia, Lymphoblastic leukemia, Microtia, Motor delay, Penis agenesis, Renal agenesis, Renal dysplasia, Renal hypoplasia, Renal insufficiency, Strabismus, Vesicoureteral refluxView all (7 more) |
|
345
|
|
|
PBX homeobox 2 |
G17, HOX12, PBX2MHC |
|
|
346
|
|
|
Pyruvate carboxylase |
PCB |
African burkitt`s lymphoma, Autism, Bipolar disorder, Burkitt`s lymphoma, Developmental delay, Hypoglycemia, Leukodystrophy, Lung carcinoma, Manic disorder, Mental retardation, Periventricular leukomalacia, Pyruvate carboxylase deficiency disease, Renal tubular acidosis |
|
347
|
|
|
Pterin-4 alpha-carbinolamine dehydratase 1 |
DCOH, PCBD, PCD, PHS |
|
|
348
|
|
|
Phosphodiesterase 11A |
PPNAD2 |
Adrenal hyperplasia, Anxiety disorder, Asthma, Atrophy, Congenital adrenal hyperplasia, Diabetes mellitus, Dwarfism, Hypercortisolism, Hypertension, Hypogonadism, Mental depression, Mood swings, Myopathy, Myopia, Osteopenia, Osteoporosis, Pigmented nodular adrenocortical disease, PsychosisView all (3 more) |
|
349
|
|
|
Propionyl-CoA carboxylase subunit alpha |
- |
Anemia, Cardiomyopathy, Cerebral atrophy, Developmental delay, Dwarfism, Eczema, Encephalopathy, Hyperglycinuria, Hypoglycemia, Mental retardation, Neutropenia, Osteoporosis, Pancreatitis, Pancytopenia, Propionic acidemia |
|
350
|
|
|
Propionyl-CoA carboxylase subunit beta |
- |
Anemia, Anxiety disorder, Cardiomyopathy, Cerebral atrophy, Developmental delay, Dwarfism, Eczema, Encephalopathy, Hyperglycinuria, Hypoglycemia, Mental retardation, Neutropenia, Osteoporosis, Pancreatitis, Pancytopenia, Propionic acidemiaView all (1 more) |
