|
811
|
|
|
Parvalbumin |
D22S749 |
Bipolar disorder, Chromophobe carcinoma, Clonic seizures, Tumor, Hypotonic seizures, Jacksonian seizure, Manic disorder, Oxyphilic adenoma, Papillary renal carcinoma, Psychosis, Renal carcinoma, Schizoaffective disorder, Schizophrenia, Schizophreniform disorders, Seizure |
|
812
|
|
|
PVR cell adhesion molecule |
CD155, HVED, NECL5, Necl-5, PVS, TAGE4 |
|
|
813
|
|
|
Pvt1 oncogene |
LINC00079, MIR1204HG, NCRNA00079, TP53LC09, onco-lncRNA-100 |
Allergic rhinitis, Allergic sensitization, B-cell neoplasm, Breast cancer, Breast carcinoma, Classical hodgkin lymphoma, Diffuse lymphoma, Hodgkin disease, Hodgkin lymphoma, Hodgkin lymphoma, lymphocyte depletion, Hypothyroidism, Immunoglobulin a deficiency, Lymphocytic leukemia, Lung adenocarcinoma, Lupus erythematosus, Multiple myeloma, Multiple sclerosis, Non-hodgkin`s lymphoma of central nervous system, Ovarian neoplasm, Renal carcinomaView all (5 more) |
|
814
|
|
|
Peroxisomal biogenesis factor 19 |
D1S2223E, HK33, PBD12A, PMP1, PMPI, PXF, PXMP1 |
Addison`s disease, Adrenoleukodystrophy, Atrial septal defect, Cardiomyopathy, Cataract, Central nervous system demyelination, Cerebral atrophy, Cholelithiasis, Congenital epicanthus, Cryptorchidism, Developmental delay, Developmental regression, Dolichocephaly, Double outlet right ventricle, Dwarfism, Facial paralysis, Glaucoma, Hearing loss, High palate, Hydrocephalus, Hydronephrosis, Hyperbilirubinemia, Hypertrophy of clitoris, Hypospadias, Ichthyosis, Impaired cognition, Infantile refsum disease, Liver failure, Macrocephaly, Malabsorption syndrome, Malformation of cortical development, Microcephaly, Micrognathism, Multicystic renal dysplasia, Nyctalopia, Nystagmus, Optic atrophy, Osteochondrodysplasia, Patent ductus arteriosus, Zellweger syndrome, Polymicrogyria, Posterior embryotoxon, Ptosis, Refsum disease, Renal tubular disorder, Rod-cone dystrophy, Scaphocephaly, Skeletal dysplasia, Strabismus, Ventricular septal defect, Zellweger-like syndromeView all (36 more) |
|
815
|
|
|
Peroxisomal biogenesis factor 2 |
PAF1, PBD5A, PBD5B, PMP3, PMP35, PXMP3, RNF72, ZWS3 |
Cubitus valgus, Addison`s disease, Adrenoleukodystrophy, Cardiomyopathy, Cataract, Cerebellar atrophy, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Congenital heart defects, Cryptorchidism, Developmental delay, Developmental regression, Dolichocephaly, Dwarfism, Dysarthria, 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, Multicystic renal dysplasia, Hypotonia, Nyctalopia, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Osteochondrodysplasia, Pachygyria, Zellweger syndrome, Polymicrogyria, Posterior embryotoxon, Ptosis, Refsum disease, Retinitis pigmentosa, Rod-cone dystrophy, Skeletal dysplasia, Strabismus, Ventricular septal defect, Zellweger-like syndromeView all (38 more) |
|
816
|
|
|
Paxillin |
- |
|
|
817
|
|
|
Peroxisomal biogenesis factor 5 |
PBD2A, PBD2B, PTS1-BP, PTS1R, PXR1, RCDP5 |
Cubitus valgus, Acrocephaly, Addison`s disease, Adrenoleukodystrophy, Amyotrophy, Asthma, Cardiomyopathy, Cataract, Chondrodysplasia punctata, Congenital camptodactyly, Congenital cataract, Congenital clubfoot, Congenital epicanthus, Congenital heart defects, Congenital hypoplasia of thymus, Cryptorchidism, Developmental delay, Developmental regression, Dolichocephaly, Dwarfism, Epilepsy, Esotropia, Facial paralysis, Frontal bossing, Glaucoma, Hearing loss, High palate, Hydronephrosis, Hypertrophy of clitoris, Hypospadias, Ichthyosis, Impaired cognition, Infantile refsum disease, Mental retardation, Liver failure, Macrocephaly, Malabsorption syndrome, Malformation of cortical development, Microcephaly, Micrognathism, Multicystic renal dysplasia, Nervous system diseases, Nyctalopia, Nystagmus, Optic atrophy, Osteochondrodysplasia, Peripheral neuropathy, Zellweger syndrome, Polycystic kidney disease, Polymicrogyria, Posterior embryotoxon, Ptosis, Refsum disease, Retinitis pigmentosa, Rhizomelic chondrodysplasia punctata, Rod-cone dystrophy, Sensory neuropathy, Sinus tachycardia, Skeletal dysplasia, Strabismus, Ventricular septal defect, Vertical nystagmusView all (47 more) |
|
818
|
|
|
Pyrroline-5-carboxylate reductase 1 |
ARCL2B, ARCL3B, P5C, P5CR, PIG45, PP222, PRO3, PYCR |
Agenesis of corpus callosum, Blepharophimosis, Developmental dysplasia of the hip, Congenital pectus carinatum, Cryptorchidism, Cutis laxa, De barsy syndrome, Developmental delay, Dwarfism, Dysmorphic features, Elbow flexion contracture, Frontal bossing, Gastroesophageal reflux disease, Geroderma osteodysplastica, Glaucoma, Glaucoma, congenital, Hydrocephalus, Malocclusion, Mental retardation, Microcephaly, Microcornea, Multiple congenital anomalies, Osteopenia, Osteoporosis, Posteriorly rotated ear, Progeria, Scoliosis, Strabismus, TalipesView all (14 more) |
|
819
|
|
|
Phosphate cytidylyltransferase 2, ethanolamine |
ET, SPG82 |
|
|
820
|
|
|
Glycogen phosphorylase B |
GPBB |
|
