|
961
|
|
|
Proliferation and apoptosis adaptor protein 15 |
HMAT1, HUMMAT1H, MAT1, MAT1H, PEA-15, PED, PED-PEA15, PED/PEA15 |
|
|
962
|
|
|
Polyribonucleotide nucleotidyltransferase 1 |
COXPD13, DFNB70, OLD35, PNPASE, SCA25, old-35 |
Cataract, Choreoathetosis, Combined oxidative phosphorylation deficiency, Deafness, Developmental delay, Dyskinetic syndrome, Encephalopathy, Hearing loss, Hip contracture, Hypothyroidism, Leukodystrophy, Orofacial dyskinesia, Liver carcinoma, Mental retardation, Non-syndromic sensorineural deafness, Nystagmus, Sensory neuropathyView all (2 more) |
|
963
|
|
|
Poly(A) binding protein cytoplasmic 4 |
APP-1, APP1, PABP4, iPABP |
|
|
964
|
|
|
Peroxisomal biogenesis factor 11 beta |
PEX11-BETA, PEX11beta, PEX14B |
Addison`s disease, Adrenoleukodystrophy, Cardiomyopathy, Cataract, Congenital cataract, Congenital epicanthus, Cryptorchidism, Developmental delay, Developmental regression, Dolichocephaly, Dwarfism, Facial paralysis, Glaucoma, Hearing loss, High palate, Hydronephrosis, Hypertrophy of clitoris, Hypospadias, Ichthyosis, Impaired cognition, Infantile refsum disease, Liver failure, Macrocephaly, Malabsorption syndrome, Malformation of cortical development, Mental retardation, Microcephaly, Micrognathism, Migraine, Multicystic renal dysplasia, Nyctalopia, Nystagmus, Optic atrophy, Osteochondrodysplasia, Peripheral neuropathy, Zellweger syndrome, Polymicrogyria, Polyneuropathy, Posterior embryotoxon, Ptosis, Refsum disease, Rod-cone dystrophy, Skeletal dysplasia, Sleep apnea, Strabismus, Testicular hydrocele, Ventricular septal defectView all (32 more) |
|
965
|
|
|
Peroxisomal biogenesis factor 11 alpha |
PEX11-ALPHA, PEX11alpha, PMP28, hsPEX11p |
|
|
966
|
|
|
Prominin 1 |
AC133, CD133, CORD12, MCDR2, MSTP061, PROML1, RP41, STGD4 |
Bipolar disorder, Bull`s eye macular dystrophy, Cataract, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Cone-rod dystrophy, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Dyschromatopsia, Endometrial neoplasms, Endometrial cancer, Giant cell glioblastoma, Glaucoma, Glioblastoma, Hearing loss, Hyperinsulinism, Hypogonadism, Intracranial aneurysm, Keratoconus, Leber congenital amaurosis, Age-related macular degeneration, Macular dystrophy, Mental depression, Mental retardation, Mixed tumor, mullerian, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Polydactyly, Retinal dystrophy, Retinal macular dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Stargardt disease, Usher syndromeView all (23 more) |
|
967
|
|
|
Protein Z, vitamin K dependent plasma glycoprotein |
PZ |
|
|
968
|
|
|
Period circadian regulator 3 |
FASPS3, GIG13 |
Advanced sleep phase syndrome, Bipolar disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Crohn disease, Marfan syndrome, Mental depression, Myeloid leukemia, Seasonal affective disorder, Sleep phase syndrome |
|
969
|
|
|
Period circadian regulator 2 |
FASPS, FASPS1 |
|
|
970
|
|
|
Paired like homeobox 2B |
CCHS, NBLST2, NBPhox, PMX2B |
Cardiovascular abnormalities, Congenital central hypoventilation, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Dysautonomia, Ganglioneuroblastoma, Ganglioneuroma, Gastroesophageal reflux disease, Haddad syndrome, Hearing loss, Hirschsprung disease, Hirschsprung disease ganglioneuroblastoma, Hirschsprung disease-ganglioneuroblastoma syndrome, Ileocolitis, Impaired cognition, Lung diseases, Mental retardation, Mouth abnormalities, Nervous system neoplasms, Neural crest tumor, Neuroblastoma, Ondine syndrome, Posteriorly rotated ear, Schizophrenia, Sleep apnea, StrabismusView all (12 more) |
