Disease

Persistent Fetal Circulation

About the Disease
Persistent Fetal Circulation Syndrome, also known as persistent fetal circulation, is related to congestive heart failure and hypokalemia. An important gene associated with Persistent Fetal Circulation Syndrome is FCGRT (Fc Gamma Receptor And Transporter), and among its related pathways/superpathways are Signal Transduction and Peptide hormone metabolism. The drugs Sildenafil and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include heart, placenta and brain, and related phenotypes are homeostasis/metabolism and renal/urinary system

Common Targets
TGFB1 | CPS1 | SIPA1L2 | DR1 | PTX3 | ARG1 | TBX4 | ASL | C12orf54 | NAGS | MDH1B | PFKM | KCNA5 | ANP32D | ASS1 | TRPC6 | MBL2 | NOS3 | TTLL3 | FANCA | OTC | PACC1 | ITGAM | BMPR2 | DUOXA1

疾病靶点研报
Persistent Fetal Circulation

Note: If you'd like to get a target analysis report for Persistent Fetal Circulation, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Persistent Fetal Circulation at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Ichthyosis Bullosa Of Siemens | Cryptorchidism | Osteoporosis | Inflammatory Myopathy | Tinea | Ocular Surface Squamous Neoplasia | CDKL5 Deficiency Disorder | Molybdenum Cofactor Deficiency | Myelofibrosis | Glioma | Gaucher Disease | Posterior Polar Cataract | Sweet Syndrome | Oral Lichen Planus | Microtia | Encephalopathy | Paraganglioma | Hidradenitis | Loeys-Dietz Syndrome | Alveolar Capillary Dysplasia | Syphilis | Osteoglophonic Dysplasia | Progressive Encephalopathy-optic Atrophy Syndrome | Dupuytren Disease | Schizophrenia | Sclerocornea | Kohlschutter-Tonz Syndrome | Hydrolethalus Syndrome | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Niemann-Pick Disease | Light Chain Amyloidosis | 3-methylglutaconic Aciduria Type IV | Vascular Cognitive Impairment | Spinal Muscular Atrophy Type 3 | Cluster Headache | Thrombophilia | Lichen Planus | Limb Girdle Muscular Dystrophy | Neurotoxicity | Spinocerebellar Ataxia Type 38 | Pneumonia, Bacterial | 3-methylglutaconic Aciduria Type I | Familial Cerebral Amyloid Angiopathy | Angiosarcoma Of The Breast | Hereditary Xerocytosis | Carcinoma, Squamous Cell | Hereditary Coproporphyria | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Long QT Syndrome Type 3 | Combined Deficiency Of Factor V And Factor VIII | Leri Pleonosteosis | Hyperinsulinemic Hypoglycemia | Hypogonadism | Alpha-mannosidosis | Urofacial Syndrome | Ocular Albinism Type 1 | Xeroderma Pigmentosum Variant Type | Glutaric Aciduria Type 2 | Glycogen Storage Disease Type 4 | Rheumatic Heart Disease | FG Syndrome | Palsy, Cerebral | Heimler Syndrome | Erysipelas | Adenocarcinoma | Epidermolysis Bullosa Simplex, Localized | Glycogen Storage Disease Type 5 | Trichomegaly | Gerstmann-Straussler-Scheinker Syndrome | DRESS Syndrome | Angioedema, Acquired | Hypersomnia | Charcot-Marie-Tooth Disease Type 2T | Globozoospermia | Exfoliative Dermatitis | Herpes Simplex Dermatitis | Microphthalmia | Autosomal Recessive Spastic Paraplegia Type 35 | Distal Myopathy | Fanconi Syndrome | Congenital Hypofibrinogenemia | Glycogen Storage Disease Type 3 | Hypospadias | Cancer, Colon | Early Infantile Epileptic Encephalopathy 4 | Speech Disorders | Cabezas Syndrome | Periventricular Nodular Heterotopia | Pompe Disease | Congenital Nystagmus | Renal Tubular Acidosis | Proteasome-associated Autoinflammatory Syndrome 2 | Pseudohermaphroditism | Sialidosis | Pneumonia, Viral | Pancreatitis | Chronic Neutrophilic Leukemia | Familial Male-limited Precocious Puberty | Fibromuscular Dysplasia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Hernia, Inguinal | Glycogen Storage Disease Type 6 | Epidermolytic Palmoplantar Keratoderma | Glaucomatocyclitic Crisis | Optic Neuropathy | GATA2 Deficiency | Blastomycosis | Peyronie's Disease | Hidradenitis Suppurativa | Vitelliform Macular Dystrophy | Osteogenesis Imperfecta Type IV | Varicocele | Zellweger Syndrome | Tyrosine Hydroxylase Deficiency | Exostoses | Leiomyoma | Hyperparathyroidism-jaw Tumor Syndrome | Lymphoma Lymphoblastic | Babesiosis | Cantu Syndrome | X-linked Charcot-Marie-Tooth Disease | Primary Cutaneous Amyloidosis | Pycnodysostosis | Diffuse Mesangial Sclerosis | Impulse Control Disorder | Bartsocas-Papas Syndrome | Atrioventricular Septal Defect | Fuchs Heterochromic Iridocyclitis | Encephalopathy, Ethylmalonic | Venous Insufficiency | Polycythemia Vera | Juvenile Myelomonocytic Leukemia | Hypopigmentation | Facioscapulohumeral Muscular Dystrophy Type 2 | Herpes Genitalis | Autosomal Recessive Spastic Paraplegia Type 75 | Cri-du-chat Syndrome | Osmotic Demyelination Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | 3-hydroxy-3-methylglutaric Aciduria | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Hypertension, Pulmonary | Fibrosis | Carcinoma, Transitional Cell | Tietze Syndrome | Carcinoid Syndrome | Nephritis, Interstitial | Spinocerebellar Ataxia Type 2 | Nephroblastoma | Kashin-Beck Disease | Metatropic Dysplasia | Tumoral Calcinosis | Oligodendroglioma | Hepatic Steatosis | Dysmorphophobia | Asthma, Nocturnal | Glutaric Aciduria Type 1 | Epilepsy Of Infancy With Migrating Focal Seizures | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Camurati-Engelmann Disease | Fukuyama Congenital Muscular Dystrophy | X-linked Creatine Transporter Deficiency | Pathological Gambling | Patent Ductus Arteriosus | Crohn's Disease | Congenital Dyserythropoietic Anemia Type 1 | Protein S Deficiency | Anal Fissure | Colorectal Adenoma | Diffuse Palmoplantar Keratoderma | Spinocerebellar Ataxia Type 21 | Chondrodysplasia Punctata 1, X-linked Recessive | Otitis Externa | Retinoschisis | Mucolipidosis Type III | Papillorenal Syndrome | Cranioectodermal Dysplasia | Facioscapulohumeral Muscular Dystrophy | Chiari Malformation Type I | Discoid Lupus Erythematosus | Tyrosinemia Type 1 | Pyelonephritis | Skin Fragility-woolly Hair Syndrome | Neurofibromatosis | Familial Isolated Hyperparathyroidism | Mood Disorder | Temtamy Preaxial Brachydactyly Syndrome | Bartter Syndrome | Focal Segmental Glomerulosclerosis | Saethre-Chotzen Syndrome | Precocious Puberty | Hypoglycemia | Primary Hyperoxaluria Type 3 | Hypermetropia | Pineoblastoma | Agranulocytosis | Waardenburg Syndrome Type 2A | Early Infantile Epileptic Encephalopathy | Cholangitis | Primary Torsion Dystonia | Heart Failure | Diabetes Gestational | HUPRA Syndrome | Bernard-Soulier Syndrome | Cocaine-Related Disorders | Acrodermatitis | Blepharoconjunctivitis | Mitochondrial Myopathy | Sickle Cell Anemia | Gangliosidosis | Congenital Adrenal Hyperplasia | Epilepsy, Generalized | Rhabdomyosarcoma, Alveolar | Takenouchi-Kosaki Syndrome | Trachoma | Adams-Oliver Syndrome | Hepatorenal Syndrome | Hypolipoproteinemia | Muckle-Wells Syndrome | Mucolipidosis Type IV | Retinal Dystrophy, Early-onset Severe | Oculocutaneous Albinism Type 2 | Preaxial Polydactyly | Persistent Hyperplastic Primary Vitreous | Galactosialidosis | Gardner Syndrome | Keratoacanthoma | Neuroma | Jalili Syndrome | Bainbridge-Ropers Syndrome | Adult Polyglucosan Body Disease | Corneal Dystrophy And Perceptive Deafness | Hemochromatosis Type 1 | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Priapism | Photosensitivity | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Thromboembolism | Dementia, Vascular | Methemoglobinemia | Otopalatodigital Syndrome Type 2 | Non-Langerhans Cell Histiocytosis | Strabismus | VACTERL/VATER Association | Goiter, Nodular | Renal Hypouricemia | Neuroendocrine Cancer | Leber Congenital Amaurosis | Majeed Syndrome | Oguchi Disease-2 | Best Macular Dystrophy | Cerebrovascular Disorders | Benign Familial Neonatal Convulsions | Barrett Esophagus | Connective Tissue Disorders | Protein C Deficiency | Bloom Syndrome | Charcot-Marie-Tooth Disease, Type 6 | Central Pain Syndrome | Choriocarcinoma | Sick Sinus Syndrome | Retinal Vasculitis | Dermatofibrosarcoma | Myelomeningocele | Tangier Disease | Homocystinuria | Heroin Dependence | Diabetes Type 2 | Rhabdoid Tumor | Retinitis Pigmentosa | Hypoplastic Left Heart Syndrome | Thalassemia, Beta | Mucolipidosis | Reye Syndrome | Focal Dermal Hypoplasia | Persistent Fetal Circulation | Nicolaides-Baraitser Syndrome | Infantile Spasm | Agammaglobulinemia | Acute Generalized Exanthematous Pustulosis | Cockayne Syndrome | Phenylketonuria | Leprosy | Chronic Inflammatory Demyelinating Polyneuropathy | Ebstein Anomaly | Congenital Myopathy | Familial Digital Arthropathy-brachydactyly | Crouzon Syndrome With Acanthosis Nigricans | Bronchitis, Chronic | Asplenia | Open-angle Glaucoma | Rickets | Pityriasis Rubra Pilaris | Coronary Heart Disease | Gastritis, Atrophic | Sclerosing Cholangitis | Pseudomyxoma Peritonei | Toxoplasmosis | Branchiootorenal Syndrome | Eating Disorder | Anorectal Fistula | Primary Aldosteronism | Hereditary Sensory Neuropathy Type 1 | Androgen Insensitivity | Glutathione Synthetase Deficiency | Osteochondrosis | Meningioma | Cerebellar Ataxia, Cayman Type | Hemosiderosis | Chediak-Higashi Syndrome | Neural Tube Defect | Nemaline Myopathy | Pleural Tuberculosis | Rothmund-Thomson Syndrome | Systemic Lupus Erythematosus | Autism | Hereditary Spherocytosis | Bare Lymphocyte Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | D-2-Hydroxyglutaric Aciduria | Pulmonary Capillary Hemangiomatosis | Alpers Syndrome | Metachondromatosis | Focal Facial Dermal Dysplasia | Diamond-Blackfan Anemia | Benign Familial Pemphigus | Prolymphocytic Leukemia | Giant Axonal Neuropathy | Hypobetalipoproteinemias | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Acne Vulgaris | Inflammatory Joint Disease | Epilepsy | Saul-Wilson Syndrome | Frank-ter Haar Syndrome | Depression | Glycogen Storage Disease Type 9 | Porphyria Cutanea Tarda | Aceruloplasminemia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Carcinoma, Small Cell | Allan-Herndon-Dudley Syndrome | Macrophagic Myofasciitis | Adrenal Insufficiency | Metaphyseal Chondrodysplasia, Schmid Type | Relapsing Polychondritis | Schwannomatosis | Vitamin K Deficiency | Olmsted Syndrome | Autoimmune Hemolytic Anemia | 3C Syndrome | Leukocyte Adhesion Deficiency Type 1 | Cerebrotendinous Xanthomatosis | Spondylo-ocular Syndrome | Scabies | Adenoma, Pituitary | Chronic Thromboembolic Pulmonary Hypertension | Reticular Dysgenesis | Carbonic Anhydrase VA Deficiency | Diabetes Insipidus | Non-epidermolytic Palmoplantar Keratoderma | Galactosemia | Chudley-McCullough Syndrome | Gnathodiaphyseal Dysplasia | Renpenning Syndrome | Angioedema | Neuroectodermal Tumors, Primitive | Membranous Nephropathy | Tinea Versicolor | Cardiac Sarcoidosis | Adenosine Deaminase Deficiency | Congenital Disorders Of Glycosylation Type II | Motor Neuron Diseases | Osteosarcoma | Hepatitis, Autoimmune | Learning Disability | Narcolepsy | Transcobalamin Deficiency | Desbuquois Syndrome | Diverticulitis | Charcot-Marie-Tooth Disease Type 3 | Ganglioneuroma | Smith-Lemli-Opitz Syndrome | Chylomicron Retention Disease | VEXAS Syndrome | Zollinger-Ellison Syndrome | Chronic Granulomatous Disease | Infantile Nephropathic Cystinosis | Peutz-Jeghers Syndrome | Histoplasmosis | Spondylometaphyseal Dysplasia | Stroke, Ischemic | Myositis | Mitochondrial DNA Depletion Syndrome 13 | Osteogenesis Imperfecta Type II | Danon Disease | Growth Hormone Excess | Urea Cycle Disorder | Osteomalacia | Postpoliomyelitis Syndrome