|
691
|
|
|
Protocadherin alpha 1 |
PCDH-ALPHA1 |
|
|
692
|
|
|
Prolactin |
GHA1 |
Adenocarcinoma, Adenoma, Anemia, Autism, Basal ganglia diseases, Benign prostatic hyperplasia, Carcinoma, Catalepsy, Congestive heart failure, Endometrioma, Endometriosis, Erectile dysfunction, Extrapyramidal disease, Fetal resorption, Frigidity, Gynecomastia, Heart failure, Hyperprolactinemia, Hypoactive sexual desire disorder, Hypogonadism, Hypogonadotropic hypogonadism, Hypopituitarism, Lenticulostriate disorders, Leydig cell tumor, Lupus erythematosus, Macroprolactinoma, Microprolactinoma, Mood disorder, Myocardial infarction, Nonbacterial verrucal endocardiosis, Orgasmic disorder, Papillary adenoma, Parkinson disease, Parkinsonian disease, Phobic anxiety disorder, Pituitary adenoma, Pituitary neoplasms, Pituitary carcinoma, Prolactinoma, Prostatic adenoma, Prostatic hyperplasia, Prostatic hypertrophy, Psychosexual disorders, Pubertal gynecomastia, Puerperal disorders, Ramsay hunt paralysis syndrome, Schizophrenia, Sexual arousal disorder, Sheehan syndrome, Somatotroph adenoma, SubfertilityView all (36 more) |
|
693
|
|
|
Prolactin receptor |
HPRL, MFAB, RI-PRLR, hPRLrI |
Anaplastic carcinoma, Autism, Carcinoma, Endometrioma, Endometriosis, Female hypogonadism syndrome, Fibroadenoma of breast, Hyperprolactinemia, Miscarriage, Multiple fibroadenomas of the breast, Osteopenia, Osteoporosis |
|
694
|
|
|
Prion protein (Kanno blood group) |
ASCR, AltPrP, CD230, CJD, GSS, KURU, PRIP, PrP, PrP27-30, PrP33-35C, PrPc, p27-30 |
Action myoclonus-renal failure syndrome, Akinetic mutism, Alzheimer disease, Alzheimer-like prion disease, Amyloidosis of peripheral nerves, Anxiety disorder, Aphasia, Apraxia, Attention deficit hyperactivity disorder, Cerebellar ataxia, Cerebellar atrophy, Cerebral amyloid angiopathy, Cerebral cortical atrophy, Creutzfeldt-jakob disease, Delusions, Dementia, Dentatorubral pallidoluysian atrophy, Dysarthria, Dysautonomia, Dysphagia, Dyssomnia, Epileptic encephalopathy, Fatal insomnia, Gastric cancer, Gerstmann-straussler-scheinker syndrome, Hallucinations, Hemiplegia, Hepatolenticular degeneration, Huntington disease-like, Hypersomnia, Inclusion-body disease, Kuru, May-white syndrome, Mental depression, Mood disorder, Mood swings, Movement disorders, Myoclonic epilepsy, Nystagmus, Nystagmus associated with disorder of the vestibular system, Parkinson disease, Prostatic neoplasms, Prostate cancer, Prp systemic amyloidosis, Psychosis, Senile dementia, Senile plaques, Sleep disorders, Specific learning disorder, Spongiform encephalopathy with neuropsychiatric features, Sporadic fatal insomnia, Stomach neoplasms, Trigeminal neuralgiaView all (38 more) |
|
695
|
|
|
Protein C, inactivator of coagulation factors Va and VIIIa |
APC, PC, PROC1, THPH3, THPH4 |
Asthma, Cerebral palsy, Congenital thrombotic disease, Developmental delay, Disseminated intravascular coagulation, Drachtman weinblatt sitarz syndrome, Gangrene, Hereditary thrombophilia, Hypertension, Non rare thrombophilia, Protein c deficiency, Purpura fulminans, Septicemia, Superficial thrombophlebitis, Thrombophilia, Thrombosis, Venous insufficiencyView all (2 more) |
|
696
|
|
|
Proline dehydrogenase 1 |
HSPOX2, PIG6, POX, PRODH1, TP53I6 |
Bipolar disorder, Breast cancer, Developmental delay, Disorder of amino acid metabolism, Hyperglycinuria, Hyperprolinemia, Inherited errors of amino acid metabolism, Kidney disease, Kidney failure, Mental retardation, Nervous system disorder, Proline dehydrogenase deficiency, Prolinuria, Schizophrenia, Status epilepticus, Stereotyped behaviorView all (1 more) |
|
697
|
|
|
PROP paired-like homeobox 1 |
CPHD2, PROP-1 |
Agenesis of corpus callosum, Central hypothyroidism, Congenital exomphalos, Developmental delay, Dwarfism, Dyssomnia, Ectopic anterior pituitary gland, Holoprosencephaly, Hypoglycemia, Hypoglycemic seizures, Hypogonadism, Hypogonadotropic hypogonadism, Hypothyroidism, Mental retardation, Non-acquired panhypopituitarism, Oral cleft, Osteopenia, Osteoporosis of vertebrae, Panhypopituitarism, Pituitary dwarfism, Pituitary hormone deficiency, Polydactyly, Septo-optic dysplasia, Sleep disordersView all (9 more) |
|
698
|
|
|
Protein S |
PROS, PS21, PS22, PS23, PS24, PS25, PSA, THPH5, THPH6 |
Activated protein c resistance, Arthritis, Colorectal cancer, Disseminated intravascular coagulation, Gangrene, Hereditary thrombophilia, Juvenile arthritis, Non rare thrombophilia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Protein s deficiency, Respiratory distress syndrome, Retinal diseases, Sagittal sinus thrombophlebitis, Sagittal sinus thrombosis, Septic phlebitis, sagittal sinus, Still disease, Superficial thrombophlebitis, Thrombophilia, Thrombosis, Venous insufficiencyView all (6 more) |
|
699
|
|
|
Par-3 family cell polarity regulator |
ASIP, Baz, PAR3, PAR3alpha, PARD-3, PARD3A, PPP1R118, SE2-5L16, SE2-5LT1, SE2-5T2 |
|
|
700
|
|
|
Prospero homeobox 1 |
- |
|
