|
321
|
|
|
Progestagen associated endometrial protein |
GD, GdA, GdF, GdS, PAEG, PEP, PP14, ZIF-1 |
|
|
322
|
|
|
Platelet activating factor acetylhydrolase 1b regulatory subunit 1 |
LIS1, LIS2, MDCR, MDS, NudF, PAFAH |
17p13.3 duplication syndrome, Agyria, Camptodactyly of fingers, Cardiovascular abnormalities, Cerebellar hypoplasia, Cerebral cortical atrophy, Developmental dysplasia of the hip, Congenital epicanthus, Congenital hypoplasia of penis, Congenital omphalocele, Developmental delay, Dysmorphic features, Frontal bossing, High palate, Hypoplasia of corpus callosum, Kidney disease, Lissencephaly, Mental depression, Mental retardation, Microstomia, Miller dieker syndrome, Mood disorder, Pachygyria, Schizophrenia, Spastic tetraparesis, Subcortical band heterotopiaView all (11 more) |
|
323
|
|
|
Phospholipase A2 group III |
GIII-SPLA2, SPLA2III, sPLA2-III |
|
|
324
|
|
|
Peroxiredoxin 1 |
MSP23, NKEF-A, NKEFA, PAG, PAGA, PAGB, PRX1, PRXI, TDPX2 |
Anemia, Asbestosis, Cerebral cortical atrophy, Cystathioninemia, Delirium, Dementia, Developmental delay, Esophagus neoplasm, Gamma-cystathionase deficiency, Hemolytic uremic syndrome, Homocystinuria, Hydrocephalus, Kidney disease, Liver carcinoma, Lung carcinoma, Lung neoplasms, Lung cancer, Macrotia, Mental retardation, Methylmalonic acidemia with homocystinuria, Microcephaly, Neutropenia, Nystagmus, Renal insufficiency, Retinitis pigmentosaView all (10 more) |
|
325
|
|
|
Phenylalanine hydroxylase |
PH, PKU, PKU1 |
Anxiety disorder, Aortic coarctation, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Bladder exstrophy, Brachydactyly, Cataract, Clinodactyly, Congenital central hypoventilation, Congenital epicanthus, Developmental delay, Double outlet right ventricle, Eczema, Esophageal atresia, High palate, Hyperphenylalaninemia, Hypopigmentation disorder, Hypoplasia of corpus callosum, Hypoplastic left heart syndrome, Mental retardation, Maternal phenylketonuria, Mental depression, Microcephaly, Micrognathism, Obsessive-compulsive disorder, Paraplegia, Phenylketonuria, Psychosis, Schizophrenia, Scleroderma, Strabismus, Tetralogy of fallot, Ventricular septal defectView all (19 more) |
|
326
|
|
|
P21 (RAC1) activated kinase 1 |
IDDMSSD, PAKalpha, alpha-PAK, p65-PAK |
Breast cancer, Mammary neoplasms, Breast carcinoma, Chromophobe carcinoma, Developmental delay, Esodeviation, Frontal bossing, Gastroesophageal reflux disease, Intellectual developmental disorder with macrocephaly, seizures, and speech delay, Mental retardation, Marfan syndrome, Melanoma, Microtia, Motor delay, Neurodevelopmental disorders, Papillary renal carcinoma, Receptive language delay, Renal carcinomaView all (3 more) |
|
327
|
|
|
P21 (RAC1) activated kinase 2 |
KNO2, PAK65, PAKgamma |
|
|
328
|
|
|
P21 (RAC1) activated kinase 3 |
ARA, MRX30, MRX47, OPHN3, PAK-3, PAK3beta, XLID30, bPAK, beta-PAK |
Agenesis of corpus callosum, Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Colorectal cancer, Developmental delay, Facial paralysis, Neurosensory hearing impairment, High palate, Mental retardation, Macrocephaly, Macrotia, Meckel diverticulum, Mental retardation, x-linked, Microcephaly, Non-syndromic intellectual disability, x-linked, Obesity, Partington syndrome, Psychosis, Seizure, Syndactyly of the toesView all (6 more) |
|
329
|
|
|
Paralemmin |
PALM1 |
|
|
330
|
|
|
Patatin like domain 8, phospholipase A2 |
IPLA2-2, IPLA2G, MMLA, PNPLA-gamma, iPLA2gamma |
|
