|
751
|
|
|
Proteasome activator subunit 2 |
PA28B, PA28beta, REGbeta |
|
|
752
|
|
|
Protein phosphatase 4 regulatory subunit 3B |
FLFL2, PP4R3B, PSY2, SMEK2, smk1 |
|
|
753
|
|
|
Phosphoserine phosphatase |
PSP, PSPHD |
3-phosphoserine phosphatase deficiency, Deficiency of phosphoserine phosphatase, Developmental delay, Disorder of amino acid metabolism, Eosinophilia, Gastroesophageal reflux disease, Hypospadias, Inherited errors of amino acid metabolism, Macrostomia, Mental retardation, Microcephaly, Micrognathism, Neu-laxova syndrome, Seizure |
|
754
|
|
|
Platelet activating factor receptor |
PAFR |
|
|
755
|
|
|
Polypyrimidine tract binding protein 1 |
HNRNP-I, HNRNPI, HNRPI, PTB, PTB-1, PTB-T, PTB2, PTB3, PTB4, pPTB |
|
|
756
|
|
|
Patched 1 |
BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH, SLC65B1 |
9q22.3 microdeletion, Accessory rib, Acquired kyphoscoliosis, Agenesis of corpus callosum, Alobar holoprosencephaly, Ambiguous genitalia, Anterior segment dysgenesis, Anxiety disorder, Arachnodactyly, Arnold-chiari malformation, Asthma, Basal cell neoplasm, Brachycephaly, Brachydactyly, Brain neoplasms, Calcification of falx cerebri, Camptodactyly of fingers, Hereditary cancer syndrome, Intracranial neoplasm, Carcinoma, Carcinoma, somatic, Cardiac fibroma, Cardiac rhabdomyoma, Cataract, Cerebral primitive neuroectodermal tumor, Choanal atresia, Cleft palate and bilateral cleft lip, Congenital anomaly of neck, Congenital coloboma of iris, Congenital epicanthus, Congenital exomphalos, Rib fusion, Congenital hypoplasia of penis, Congenital kyphoscoliosis, Congenital pectus excavatum, Congenital primary aphakia, Congenital scoliosis, Cryptorchidism, Cyclocephaly, Defect of skull ossification, Delayed speech and language development, Developmental delay, Duodenal atresia, Dwarfism, Dysmorphic features, Dysphagia, Ependymoblastoma, Expressive language delay, Frontal bossing, Fused incisors, Gastrointestinal stromal tumor, Glaucoma, Gorlin syndrome, Hemangioma, Hiatal hernia, Holoprosencephaly, Hydrocephalus, Hyperopic astigmatism, Hypogonadotropic hypogonadism, Hypoplasia of corpus callosum, Hypoplasia of the maxilla, Hypoplasia of thumb, Hypothyroidism, Impaired cognition, Mental retardation, Keratocystic odontogenic tumor, Lagopthalmos, Lobar holoprosencephaly, Macrocephaly, Macrotia, Malocclusion, Medulloblastoma, Medulloepithelioma, Medullomyoblastoma, Megalencephaly, Melanocytic nevus, Metopic synostosis, Microcephaly, Microform holoprosencephaly, Microphthalmos, Microstomia, Midline interhemispheric variant of holoprosencephaly, Monosomy 9q22.3, Motor delay, Neoplasms, Nephroblastoma, Neuroectodermal tumors, Nevus, Oculodentodigital dysplasia, Oral cleft, Orbital cyst, Osteomyelitis, Otitis media, Ovarian cancer, Ovarian carcinoma, Ovarian epithelial carcinoma, Ovarian fibromata, Pancreatic neoplasm, Pancreatic cancer, Panhypopituitarism, Partial or complete agenesis of corpus callosum, Patent ductus arteriosus, Periauricular skin pits, Pierre-robin syndrome, Polydactyly, Renal agenesis, Renal hypoplasia, Retinal diseases, Rhabdomyosarcoma, Rieger syndrome, Schilbach-rott syndrome, Scoliosis, Segment dysgenesis, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Skin cancer, Skin neoplasms, Sleep apnea, Spina bifida, Spongioblastoma, Sprengel deformity, Strabismus, Syndactyly of the toes, Tetralogy of fallot, Trichotillomania, TrigonocephalyView all (111 more) |
|
757
|
|
|
Phosphatase and tensin homolog |
10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, PTENbeta, PTENgama, TEP1 |
Acrokeratosis, Activated pi3k-delta syndrome, Adenocarcinoma, Adenoma sebaceum, Anaplastic carcinoma, Anemia, Angioblastic meningioma, Angioid streaks, Angioma, Angiomatous meningioma, Anisometropia, Anxiety disorder, Aortic aneurysm, Apraxia, Arnold-chiari malformation, Asthma, Atrial septal defect, Attention deficit hyperactivity disorder, Auditory processing disorder, Autism spectrum disorder, Autism, Bannayan-riley-ruvalcaba syndrome, Benign meningioma, Brachydactyly, Brain neoplasms, Breast adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Cafe-au-lait spot, Camptodactyly of fingers, Hereditary cancer syndrome, Carcinoma, Carcinoma of the head and neck, Carcinoma of the nasal cavity and paranasal sinuses, Carcinoma of the oral cavity, Cataract, Celiac disease, Cerebellar granule cell hypertrophy and megalencephaly, Cerebelloparenchymal disorder, Cerebral convexity meningioma, Uterine cervix neoplasm, Cholangiocarcinoma, Chorioangioma, Chromophobe carcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Communicating hydrocephalus, Congenital anomaly of neck, Congenital arteriovenous malformation, Congenital bronchogenic cyst, Congenital genu recurvatum, Congenital hemihypertrophy, Congenital macrodactylia, Congenital pectus excavatum, Congestive heart failure, Conjunctival hamartoma, Cowden syndrome, Cranial nerve paralysis, Craniosynostosis, Cutis marmorata, Dermatologic disorders, Development disorder, Developmental delay, Developmental dyspraxia, Developmental regression, Diabetes insipidus, Dolichocephaly, Ductal carcinoma, Dwarfism, Dysmorphic features, Dysplastic cerebellar gangliocytoma, Endocrine gland cancer, Endometrial cancer, Endometrial neoplasms, Endometrial carcinoma, Endometrial hyperplasia, Enlarged polycystic ovaries, Epidermal nevus, Epithelioid hemangioma, Fatty liver, Fibroadenoma of breast, Fibrous meningioma, Follicular thyroid carcinoma, Fossa meningioma, Frontal bossing, Fundus coloboma, Gastric cancer, Glaucoma, congenital, Glioblastoma, Glioma, Gynecomastia, Hamartoma, Hamartomatous polyposis, Hashimoto disease, Hemangioblastic meningioma, Hemangioblastoma, Hemangioma, Hemangioma, cavernous, Hemangiopericytic meningioma, Hemimegalencephaly, Hemiplegia/hemiparesis, Hepatocellular adenoma, Hereditary breast and ovarian cancer syndrome, Hibernoma, High palate, Hydrocephalus, Hyperostosis, Hypertension, Hyperthyroidism, Hypoalbuminemia, Hypoglycemia, Hypopharyngeal carcinoma, Hypoplasia of the maxilla, Hypothyroidism, Immunoglobulin a deficiency, Impaired cognition, Infantile spasms, Mental retardation, Intestinal polyposis, Intracranial meningioma, Intrahepatic cholangiocarcinoma, Intraorbital meningioma, Intraventricular meningioma, Intussusception, Kidney cancer, Language development disorders, Laryngeal carcinoma, Leopard syndrome, Leukemia, Lhermitte-duclos disease, Lip carcinoma, Lipoma, Lipomatosis, Liver carcinoma, Liver cirrhosis, Liver fibrosis, Long qt syndrome, Lung carcinoma, Lung neoplasms, Lung cancer, Lymphangioma, Lymphoma, Macrocephaly, Macrocephaly autism syndrome, Macrocephaly-intellectual disability-autism syndrome, Macroglossia, Macrotia, Malignant meningioma, Malignant neoplasm, Hereditary cancer, Malignant uterine corpus neoplasm, Malocclusion, Marfan syndrome, Mediastinal tumor, Megakaryocytic leukemia, Melanocytic nevus, Melanoma, Meningioma, Meningothelial meningioma, Mental depression, Microcystic meningioma, Micrognathism, Microstomia, Motor delay, Motor skills disorders, Malignant neoplasm of floor of mouth, Movement disorders, Multiple congenital anomalies, Myofibrillar myopathy, Myopathy, Myopia, Nasopharyngeal carcinoma, Neoplasms, Neurodevelopmental disorders, Neuronal heterotopia, Nevus, Non-alcoholic fatty liver disease, Obesity, Obsessive-compulsive disorder, Olfactory groove meningioma, Oropharyngeal carcinoma, Osteochondrodysplasia, Ovarian neoplasm, Ovarian cancer, Ovarian carcinoma, Ovarian cysts, Ovarian epithelial carcinoma, Ovarian mucinous tumor, Palmoplantar keratoderma, Palmoplantar keratosis, Pancreatic neoplasm, Pancreatic cancer, Papillary meningioma, Papillary renal carcinoma, Papillary thyroid carcinoma, Papilloma, Paraganglioma, Parasagittal meningioma, Patent ductus arteriosus, Peritoneal carcinoma, Polycystic ovary syndrome, Polydactyly, Polymicrogyria, Polyp, Polyp of large intestine, Polyposis, Polyposis syndrome, Proptosis, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer, Protein-losing enteropathy, Proteus syndrome, Proteus-like syndrome, Psammomatous meningioma, Pten hamartoma tumor syndrome with granular cell tumor, Pten hamartoma tumor syndrome, Ptosis, Rectal prolapse, Renal carcinoma, Renal cyst, Retinal coloboma, Retinal detachment, Retinal hamartoma, Retinal nonattachment, Salivary gland carcinoma, Scoliosis, Secretory meningioma, Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome, Sezary syndrome, Shagreen patch, Sirenomelia, Skeletal dysplasia, Skin diseases, vascular, Skin lesion, Social communication disorder, Speech delay, Speech disorders, Sphenoid wing meningioma, Spinal meningioma, Carcinoma of lip, Oral cavity carcinoma, Strabismus, Strawberry nevus of skin, Subcutaneous hemorrhage, Subcutaneous lipoma, Syndactyly of fingers, Talipes, Testicular neoplasms, Testicular hydrocele, Thymus neoplasms, Thymus hyperplasia, Thyroid neoplasm, Thyroid cancer, Thyroid carcinoma, Thyroid diseases, Thyroid gland follicular adenoma, Thyroid nodule, Thyroiditis, Bladder carcinoma, Transitional meningioma, Trichilemmoma, Tumors of adrenal cortex, Vacterl association, Varicocele, Venous insufficiency, Visceral angiomatosis, Xanthomatous meningiomaView all (255 more) |
|
758
|
|
|
Prostaglandin D2 synthase |
L-PGDS, LPGDS, PDS, PGD2, PGDS, PGDS2 |
|
|
759
|
|
|
Prostaglandin E receptor 1 |
EP1 |
|
|
760
|
|
|
Prostaglandin E receptor 2 |
COX-2, EP2 |
|
