|
831
|
|
|
Prokineticin 2 |
BV8, HH4, KAL4, MIT1, PK2 |
Anxiety disorder, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Gynecomastia, Hearing loss, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mental depression, Mirror movements, Mood disorder, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Secondary physiologic amenorrhea, Skeletal dysplasia, Testicular hypogonadismView all (19 more) |
|
832
|
|
|
Pappalysin 2 |
PAPP-A2, PAPP-E, PAPPE, PLAC3, SSDA |
|
|
833
|
|
|
PBX/knotted 1 homeobox 2 |
PREP2 |
|
|
834
|
|
|
Piezo type mechanosensitive ion channel component 2 |
C18orf30, C18orf58, DA3, DA5, DAIPT, FAM38B, FAM38B2, HsT748, HsT771, MWKS |
Absence of septum pellucidum, Mallet finger, Acquired kyphoscoliosis, Agenesis of corpus callosum, Arachnodactyly, Arthrogryposis multiplex congenita, Arthrogryposis, with impaired proprioception and touch, Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome, Astigmatism, Attention deficit hyperactivity disorder, Blepharophimosis, Camptodactyly of fingers, Cerebellar hypoplasia, Clinodactyly, Congenital camptodactyly, Congenital clubfoot, Congenital contracture, Developmental dysplasia of the hip, Congenital epicanthus, Congenital finger flexion contractures, Pulmonary hypoplasia, Congenital keratoglobus, Congenital kyphoscoliosis, Congenital pectus carinatum, Congenital pectus excavatum, Connective tissue disease, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Dextrocardia, Diabetes mellitus, Distal arthrogryposis, Duane retraction syndrome, Dwarfism, Dysarthria, Dysmorphic features, Epispadias, Gordon syndrome, High palate, Hydrocephalus, Hydronephrosis, Hypospadias, Keratoconus, Lung carcinoma, Macrotia, Marden-walker syndrome, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Motor delay, Multicystic renal dysplasia, Multiple congenital anomalies, Muscular dystrophy, Hypotonia, Oculomelic amyoplasia, Optic atrophy, Penis agenesis, Posteriorly rotated ear, Ptosis, Radioulnar synostosis, Renal agenesis, Renal dysplasia, Renal hypoplasia, Scoliosis, Sheldon-hall syndrome, Situs inversus, Specific learning disorder, Spondylolysis, Strabismus, Submucosal cleft palate, Syndactyly of fingers, Talipes, Thoracolumbar scoliosis, Ventricular septal defect, Zollinger-ellison syndromeView all (62 more) |
|
835
|
|
|
PR/SET domain 1 |
BLIMP-1, BLIMP1, PRDI-BF1 |
Ankylosing spondylitis, Cholangitis, Crohn disease, Diffuse lymphoma, Inflammatory bowel disease, Lupus erythematosus, Nonbacterial verrucal endocardiosis, Psoriasis, Rheumatoid arthritis, Sjogren`s syndrome, Ulcerative colitis |
|
836
|
|
|
Phosphorylated CTD interacting factor 1 |
C20orf67, CAPAM, MT-A70, PPP1R121, hCAPAM, hPCIF1 |
|
|
837
|
|
|
PR/SET domain 16 |
CMD1LL, KMT8F, LVNC8, MEL1, PFM13 |
1p36 deletion syndrome, Abdominal migraine, Agenesis of corpus callosum, Allergic rhinitis, Aneurysm of aortic arch, Annular pancreas, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cardiomyopathy, Cardiovascular diseases, Cataract, Cerebral cortical atrophy, Confusional migraine, Congenital anomaly of neck, Congenital epicanthus, Rib fusion, Congenital hypoplasia of penis, Congestive heart failure, Coronary artery disease, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dilated cardiomyopathy, Dwarfism, Dysphagia, Eczema, Fatty liver, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Heart septal defects, Hemicrania migraine, Hemiplegia/hemiparesis, Hydronephrosis, Hypogonadism, Hypospadias, Hypothyroidism, Left ventricular noncompaction, Lipoatrophy, Lipodystrophy, Mental retardation, Microcephaly, Microstomia, Microtia, Migraine, Motion sickness, Myopathy, Neuroblastoma, Nystagmus, Obesity, Ocular albinism, Optic atrophy, Palmoplantar keratoderma, Patent ductus arteriosus, Polydactyly of toes, Biliary cirrhosis, Renal cyst, Rheumatoid arthritis, Scoliosis, Status migrainosus, Stereotyped behavior, Strabismus, Tetralogy of fallot, Ventricular noncompactionView all (51 more) |
|
838
|
|
|
PR/SET domain 14 |
PFM11 |
|
|
839
|
|
|
P53 apoptosis effector related to PMP22 |
EKVP7, KCP1, KRTCAP1, OLMS2, PIGPC1, THW, dJ496H19.1 |
Alopecia, Anhidrosis, Hearing loss, Hyperhidrosis palmaris et plantaris, Hypodontia, Hypotrichosis, Lung neoplasms, Melanoma, Mutilating palmoplantar keratoderma with periorificial keratotic plaques, Olmsted syndrome, Palmoplantar keratoderma, Skin neoplasms |
|
840
|
|
|
Prolyl 3-hydroxylase 1 |
GROS1, LEPRE1, OI8 |
|
