Postpartum Depression

About the Disease
Postpartum Depression, also known as depression, postpartum, is related to major depressive disorder and mood disorder, and has symptoms including pelvic pain and mental and behavioral signs and symptoms. An important gene associated with Postpartum Depression is CRH (Corticotropin Releasing Hormone), and among its related pathways/superpathways are Signal Transduction and Myometrial relaxation and contraction pathways. The drugs Copper and Ethinylestradiol have been mentioned in the context of this disorder. Affiliated tissues include breast, brain and thyroid, and related phenotypes are nervous system and homeostasis/metabolism

Common Targets
DRD2 | GABRA4 | NR3C1 | Estrogen receptor (nonspecified subtype) | GABRG2 | GABA(A) receptor | G5743 | TTC9B | MTHFR | OXT | SLC6A4 | GABRA1 | HTR2A | CRHR1 | TPH1 | GABRD | OXTR | HP1BP3 | CLOCK | Carbonic Anhydrase (nonspecified subtype) | PABPC1L

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Other Diseases

Withdrawal Syndrome | Macular Corneal Dystrophy | Acrodermatitis | Pulmonary Vein Stenosis | Charcot-Marie-Tooth Disease Type 2D | Spinocerebellar Ataxia Type 8 | Cellulitis | Perry Syndrome | Familial Exudative Vitreoretinopathy | Persistent Mullerian Duct Syndrome | Congenital Stationary Night Blindness | Melanoma, Uveal | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Congenital Adrenal Hyperplasia | Alazami Syndrome | Androgenic Alopecia | Schamberg Disease | Acne | Follicular Dendritic Cell Sarcoma | Palsy, Cerebral | Spinocerebellar Ataxia Type 2 | Stroke, Hemorrhagic | Glioblastoma | Osteogenesis Imperfecta | Primary Progressive Aphasia | Autosomal Recessive Bestrophinopathy | Charcot-Marie-Tooth Disease | C3 Glomerulonephritis | Mannosidase Deficiency Diseases | Depression | Ehlers-Danlos Syndrome | Bullous Pemphigoid | Pontocerebellar Hypoplasia | Desmosterolosis | Learning Disability | Rhabdomyosarcoma | Splenomegaly | VACTERL/VATER Association | Ichthyosis Hystrix, Curth-Macklin Type | Alkaptonuria | Becker Muscular Dystrophy | Osteogenesis Imperfecta Type I | Megalencephaly | Optic Atrophy 2 | Mitochondrial Myopathy | Combined Malonic And Methylmalonic Acidemia | Chondrosarcoma | Pupil Disorders | Polymicrogyria | Hypercholesterolemia, Familial | Hyperandrogenemia | Episodic Ataxia Type 1 | Thrombocytopenia | Eclampsia | Glycogen Storage Disease Type 6 | Glanzmann Thrombasthenia | Lymphedema-distichiasis Syndrome | Encephalopathy, Glycine | Pachyonychia Congenita | Tumoral Calcinosis | Gerstmann-Straussler-Scheinker Syndrome | Achondrogenesis | Gnathodiaphyseal Dysplasia | Isovaleric Acidemia | Fibrosarcoma | Jawad Syndrome | Spinocerebellar Ataxia Type 6 | Persistent Fetal Circulation | Motor Neuron Diseases | Corneal Neovascularization | Neurofibromatosis-Noonan Syndrome | Nemaline Myopathy | Cheilitis | Xeroderma Pigmentosum Variant Type | Richter's Syndrome | Cysticercosis | Spinocerebellar Ataxia | Treacher Collins Syndrome | Stevens-Johnson Syndrome | Dystonia | Leishmaniasis, Visceral | Li-Fraumeni Syndrome | Blepharoconjunctivitis | CHARGE Syndrome | Asperger Syndrome | High Molecular Weight Kininogen Deficiency | Neurodevelopmental Disorders | Pneumoconiosis | Reflex Epilepsy | Spermatocele | Hepatitis E | Kindler Syndrome | Campomelic Dysplasia | N-acetylglutamate Synthase Deficiency | Hyperhomocysteinemia | Oguchi Disease-2 | Spinocerebellar Ataxia Type 23 | Epidermolytic Palmoplantar Keratoderma | Tyrosinemia Type 2 | Basan Syndrome | Restrictive Dermopathy | Raine Syndrome | Rash | Hydrolethalus Syndrome | Pompe Disease | COACH Syndrome | Neuromyotonia | Absence Epilepsy | Leukoplakia | Retinopathy, Diabetic | HELLP Syndrome | Varices | Glaucoma, Congenital | Hepatopulmonary Syndrome | Hyperprolactinemia | Hypertensive Retinopathy | Allan-Herndon-Dudley Syndrome | Gyrate Atrophy Of The Choroid And Retina | Warsaw Breakage Syndrome | Diffuse Palmoplantar Keratoderma | Gastrointestinal Disorders | MIRAGE Syndrome | Ebstein Anomaly | Osteomyelitis | Neuronal Ceroid Lipofuscinosis | Infantile Spasm | Anti-NMDA Receptor Encephalitis | Exfoliative Dermatitis | Vitiligo | Infantile Neuroaxonal Dystrophy | Schnyder Crystalline Corneal Dystrophy | Neurofibromatosis Type 2 | Ghosal Syndrome | Acrodermatitis Enteropathica | Still Disease | Glucagonoma | Methylmalonic Aciduria And Homocystinuria, CblC Type | Ganglioglioma | Syphilis | Myocarditis | Microcephaly, Seizures, And Developmental Delay | Papillon-Lefevre Syndrome | Adenoma, Pleomorphic | Charcot-Marie-Tooth Disease Type 4E | Anorectal Fistula | Acute Leukemia | Pemphigus | Ellis-Van Creveld Syndrome | Lymphedema | Cold Agglutinin Disease | Brooke-Spiegler Syndrome | Spinocerebellar Ataxia Type 13 | Trigonocephaly | Insulinoma | Epidermolysis Bullosa Simplex, Localized | Pregnancy, Ectopic | Werner's Syndrome | Lactose Intolerance | Myasthenia | Chondrodysplasia Punctata 1, X-linked Recessive | Seborrheic Dermatitis | Birk-Barel Syndrome | Hyperinsulinemic Hypoglycemia | Schistosomiasis Mansoni | Cervical Dystonia | Multiple Sulfatase Deficiency | Blau Syndrome | Vitreoretinal Degeneration, Snowflake Type | Hyper IgE Syndrome | Bernard-Soulier Syndrome | Temporal Lobe Epilepsy | Batten Disease | Bladder Exstrophy | Gilbert Syndrome | Varicocele | Juvenile Xanthogranuloma | Corneal Ulcer | Nanophthalmos | Cantu Syndrome | Tetraplegia | Tietze Syndrome | Autosomal Recessive Congenital Ichthyosis | Familial Dysautonomia | 3-methylglutaconic Aciduria Type I | Blue Rubber Bleb Nevus Syndrome | Primary Progressive Nonfluent Aphasia | Retinoschisis | Chloridorrhea, Congenital | Goldenhar Syndrome | Familial Hyperaldosteronism | Chanarin-Dorfman Syndrome | Synovitis | Vertebrobasilar Insufficiency | Multicystic Renal Dysplasia | Primary Biliary Cholangitis | Ocular Albinism Type 1 | Keloid | Juvenile Myoclonic Epilepsy | Nasodigitoacoustic Syndrome | Zollinger-Ellison Syndrome | Meckel-Gruber Syndrome | Bainbridge-Ropers Syndrome | Diarrhea | Methemoglobinemia Type IV | Apparent Mineralocorticoid Excess Syndrome | Kernicterus | Hypotension, Orthostatic | Growth Hormone Excess | Kallmann Syndrome | Frontometaphyseal Dysplasia | Pouchitis | Inflammatory Joint Disease | Wolcott-Rallison Syndrome | Epidermolytic Ichthyosis, Annular | Neuromuscular Disorders | Cancer, Colon | Lafora Disease | Keratitis | Hepatitis, Alcoholic | Takayasu's Arteritis | Retinal Dystrophy | Lymphoma Lymphoblastic | Non-proliferative Diabetic Retinopathy | Amblyopia | Galactosemia | Alzheimer Disease, Late Onset | Mastitis | Osteosarcoma | Diabetes Type 2 | Pitt-Hopkins Syndrome | Familial Hemiplegic Migraine | Choroideremia | Chordoid Glioma | ACTH-independent Macronodular Adrenal Hyperplasia | Tremor | Epidermolysis Bullosa Acquisita | Speech Disorders | Hairy Cell Leukemia | Supravalvular Aortic Stenosis | Arteriovenous Malformations | Fibrodysplasia Ossificans Progressiva | Myelitis | Partington Syndrome | Gallstones | Hypermetropia | Xeroderma Pigmentosum | Heterotaxy | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Galactosialidosis | Potocki-Shaffer Syndrome | Axenfeld-Rieger Syndrome | Infantile Liver Failure Syndrome 1 | Wieacker-Wolff Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Sialoadenitis | Dupuytren Disease | Canavan Disease | Acute Tubular Necrosis | Tuberculous Meningitis | Hypopigmentation | Metachromatic Leukodystrophy | Cholangiocarcinoma | Mitochondrial DNA Depletion Syndrome | Congenital Poikiloderma | Periventricular Leukomalacia | Papulopustular Rosacea | Cardiomyopathy, Peripartum | Monilethrix | Astrocytoma | McKusick Type Metaphyseal Chondrodysplasia | Hyperinsulinism-hyperammonemia Syndrome | Sensorineural Hearing Loss | Papillorenal Syndrome | Cockayne Syndrome | Histiocytosis | Polycystic Liver | Infertility | Microcephalic Primordial Dwarfism | Van Der Knaap Disease | Granuloma Annulare | Eccrine Porocarcinoma | Autoimmune Polyendocrinopathy Syndrome Type I | Macrodactyly | Proctitis | Androgen Insensitivity | Premenstrual Syndrome | Exocrine Pancreatic Insufficiency | Congenital Dysfibrinogenemia | Ornithine Transcarbamylase Deficiency | Leukocyte Adhesion Deficiency | Neurogenic Bladder | Congenital Lipoid Adrenal Hyperplasia | Heimler Syndrome | Optic Neuropathy, Anterior Ischemic | Motion Sickness | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Gastric Atrophy | Pemphigoid | 3-methylglutaconic Aciduria | Autoimmune Autonomic Ganglionopathy | Sporadic Inclusion Body Myositis | Echinococcosis | Nephritis, Interstitial | Spinocerebellar Ataxia Type 20 | Nail-Patella Syndrome | Okihiro Syndrome | Osteogenesis Imperfecta Type III | Spitzoid Melanoma | Carpal Tunnel Syndrome | Chondrodysplasia Punctata | Tylosis With Esophageal Cancer | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Colitis, Microscopic | Milk Allergy | Tyrosine Hydroxylase Deficiency | Sleep Apnea | Epilepsy | Common Variable Immunodeficiency | Angioimmunoblastic T-cell Lymphoma | Parapsoriasis | Sick Sinus Syndrome 1 | Chronic Idiopathic Myelofibrosis | Pneumonia, Mycoplasma | Peeling Skin Syndrome Type B | Meningioma | Chronic Beryllium Disease | Anorchia | Hypotrichosis | Pontocerebellar Hypoplasia Type 7 | Actinomycetoma | Episodic Ataxia | Corneal Dystrophy | NDH Syndrome | Systemic Mastocytosis | Hemochromatosis | Relapsing Polychondritis | Early Infantile Epileptic Encephalopathy 28 | Periodic Limb Movement Disorder | Hemimegalencephaly | Narcolepsy | Palmoplantar Keratoderma | Hypertriglyceridemia | Alpha-1 Antitrypsin Deficiency | Cocaine-Related Disorders | Dystrophy, Cone-rod | Glioblastoma Multiforme | Niemann-Pick Disease, Type C | Multiple Epiphyseal Dysplasia | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Aneurysm, Thoracic Aortic | Adenosine Deaminase Deficiency | Pulmonary Veno-occlusive Disease | Waardenburg Syndrome Type 4 | Usher Syndrome | Bartter Syndrome | Sezary Syndrome | Pyruvate Dehydrogenase Deficiency | Aneurysm, Abdominal Aortic | Hashimoto Thyroiditis | Sarcoma, Ewing | Acromicric Dysplasia | DEND Syndrome | Measles | Obesity | Brachydactyly | Pyruvate Decarboxylase Deficiency | Hemolytic Uremic Syndrome, Atypical | Early Infantile Epileptic Encephalopathy 13 | Presbyopia | Tatton-Brown-Rahman Syndrome | Oligodendroglioma | Congenital Diaphragmatic Hernia | Fabry's Disease | Pleurisy | Usher Syndrome Type III | HIBCH Deficiency | Essential Fructosuria | Epidermolysis Bullosa Dystrophica | Asthma, Nocturnal | Cutaneous Lupus Erythematosus | Adrenomyeloneuropathy | Trachoma | X-linked Acrogigantism | Primary Erythromelalgia | Primrose Syndrome | Arthrogryposis | Cirrhosis | Apert Syndrome | Neurocutaneous Melanocytosis | Waardenburg Syndrome Type 2E | Sarcoma, Alveolar Soft Part | Stargardt Disease | Gangliosidosis | Meningococcal Infections | Tracheal Disorders | Pernicious Anemia | Rubeosis Iridis | Renal Hypouricemia | Duane Retraction Syndrome | CDKL5 Deficiency Disorder