|
191
|
|
|
Pyridoxal dependent decarboxylase domain containing 1 |
LP8165 |
|
|
192
|
|
|
PDS5 cohesin associated factor B |
APRIN, AS3, CG008 |
|
|
193
|
|
|
Pogo transposable element derived with ZNF domain |
MRD37, WHSUS, ZNF280E, ZNF635, ZNF635m |
Astigmatism, Autism spectrum disorder, Autism, Brachycephaly, Brachydactyly, Central visual impairment, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Congenital coloboma of iris, Congenital diaphragmatic hernia, Congenital heart defects, Developmental delay, Dwarfism, Dyscognitive seizures, Dysmorphic features, Expressive language delay, Febrile seizures, Gastroesophageal reflux disease, Hearing loss, High palate, Hyperopia, Hypoglycemic seizures, Hypoplasia of corpus callosum, Hypothyroidism, Mental retardation, Macrostomia, Malocclusion, Microcephaly, Microstomia, Movement disorders, Multiple congenital anomalies, Myopia, Neurodevelopmental disorders, Obesity, Obsessive-compulsive disorder, Optic atrophy, Posteriorly rotated ear, Rod-cone dystrophy, Seizure, Sensorineural hearing loss, Sleep apnea, Stereotyped behavior, Strabismus, Subcortical cerebral atrophy, Vitiligo, White-sutton syndromeView all (32 more) |
|
194
|
|
|
Plexin D1 |
CHTD9, PLEXD1 |
Arthrogryposis multiplex congenita, Autism, Brachydactyly, Cafe-au-lait spot, Camptodactyly of fingers, Breast aplasia, Congenital clubfoot, Congenital epicanthus, Dysphagia, Facial paralysis, Heart failure, High palate, Hypogonadotropic hypogonadism, Microdontia, Micrognathism, Mobius syndrome, Moebius syndrome, Motor delay, Persistent truncus arteriosus, Ptosis, Strabismus, Syndactyly of fingersView all (7 more) |
|
195
|
|
|
PHD finger protein 8 |
JHDM1F, KDM7B, MRXSSD, ZNF422 |
Cryptorchidism, Dysmorphic features, Mental disorders, Mental retardation, Mental retardation, x-linked, Multiple congenital anomalies, Polydactyly, Psychosis, Scoliosis, Syndromic mental retardation, x-linked, Synophrys |
|
196
|
|
|
PAS domain containing serine/threonine kinase |
PASKIN, STK37 |
|
|
197
|
|
|
Pleckstrin homology like domain family B member 1 |
LL5A, LL5alpha, OI23 |
|
|
198
|
|
|
Peptidase, mitochondrial processing subunit alpha |
Alpha-MPP, CLA1, CPD3, INPP5E, MAS2, P-55, SCAR2 |
Cataract, Cerebellar hypoplasia, Cerebelloparenchymal disorder, Developmental delay, Dysarthria, Hydrocephalus, Hypertrophic cardiomyopathy, Malabsorption syndrome, Mental retardation, Movement disorders, Nystagmus, Ocular albinism, Optic atrophy, Scoliosis, Spinocerebellar ataxia |
|
199
|
|
|
Pleckstrin homology and RUN domain containing M2 |
SKIP |
|
|
200
|
|
|
Proline rich coiled-coil 2C |
BAT2-iso, BAT2D1, BAT2L2, XTP2 |
|
