Disease

Congenital Sodium Diarrhea

About the Disease
Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies, also known as diarrhea 3, secretory sodium, congenital, syndromic, is related to diarrhea 8, secretory sodium, congenital and diarrhea, and has symptoms including diarrhea and watery diarrhea. An important gene associated with Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies is SPINT2 (Serine Peptidase Inhibitor, Kunitz Type 2). Affiliated tissues include olfactory bulb and bone, and related phenotypes are macrocephaly and low-set ears

Common Targets
SPINT2 | SLC9A3

疾病靶点研报
Congenital Sodium Diarrhea

Note: If you'd like to get a target analysis report for Congenital Sodium Diarrhea, 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 Congenital Sodium Diarrhea at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Juvenile Hyaline Fibromatosis | Exostoses | Noonan Syndrome-like Disorder With Loose Anagen Hair | Tetanus | Hepatitis E | Familial Mediterranean Fever | Congenital Bilateral Absence Of Vas Deferens | Centronuclear Myopathy | Astrocytoma, Anaplastic | Metabolic Diseases | Androgen Insensitivity | Infantile Neuroaxonal Dystrophy | Hereditary Spastic Paraplegia | Neuroblastoma | Osteitis | Polycystic Kidney, Autosomal Recessive | Neurofibrosarcoma | Tibial Muscular Dystrophy | Lymphoma | Kabuki Syndrome 2 | Keratocystic Odontogenic Tumor | Hyperkalemic Periodic Paralysis | Cutaneous Angiosarcoma | Vertigo | Kohlschutter-Tonz Syndrome | Hereditary Sensory And Autonomic Neuropathy | Parkinson's Disease | Hemimegalencephaly | Hemangioblastoma | Congenital Sodium Diarrhea | Focal Cortical Dysplasia Type 2 | Hyperparathyroidism, Primary | Congenital Aniridia | Dowling-Degos Disease | Saethre-Chotzen Syndrome | Esophageal Adenocarcinoma | Peritonitis | Spinal Muscular Atrophy Type 3 | Meningeal Melanocytoma | Thrombotic Microangiopathy | Autosomal Recessive Spastic Paraplegia Type 54 | Citrullinemia | Inflammatory Linear Verrucous Epidermal Nevus | Steel Syndrome | Klinefelter Syndrome | Eclampsia | Myelodysplasia | Otitis Externa | Anorectal Fistula | Hypertelorism | Acute Leukemia | Cholelithiasis | Gliosarcoma | Angioedema | Primary Progressive Nonfluent Aphasia | Cryoglobulinemia | Microphthalmia, Syndromic 7 | Sporadic Inclusion Body Myositis | Bursitis | Hypopituitarism | Osteoporosis, Postmenopausal | Neurofibroma, Plexiform | Corneal Dystrophy | Splenomegaly | Papillorenal Syndrome | Chronic Granulomatous Disease, X-linked | Specific Granule Deficiency | Chronic Kidney Disease | Pierson Syndrome | Fetal Akinesia Deformation Sequence | Hepatic Veno-occlusive Disease | Hypercalcemia | Macular Degeneration | Beckwith-Wiedemann Syndrome | Agnathia-Otocephaly Complex | Hyperthermia, Malignant | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Christianson Syndrome | Amebiasis | Ghosal Syndrome | Exocrine Pancreatic Insufficiency | Angelman Syndrome | Guttate Psoriasis | Mitochondrial Cytopathy | Impulse Control Disorder | Rash | Incontinentia Pigmenti | Absence Epilepsy | Spastic Paraplegia Type 7 | Warsaw Breakage Syndrome | Tangier Disease | Pulmonary Alveolar Microlithiasis | Sleep Disorder | Spondyloepiphyseal Dysplasia Tarda, X-linked | Chromosome 17q21.31 Deletion Syndrome | Neurofibromatosis-Noonan Syndrome | Giant Axonal Neuropathy | Hypertension, Pulmonary | CHOPS Syndrome | Cutis Laxa | Split Hand-foot Malformation | Phenylketonuria II | Primary Biliary Cholangitis | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Hypertension | Chronic Lymphocytic Leukemia | Spinocerebellar Ataxia Type 38 | Scleroderma, Diffuse | Tyrosine Hydroxylase Deficiency | Liver Diseases | Keratosis, Actinic | DICER1 Syndrome | Sitosterolemia | Craniosynostosis | Glycogen Storage Disease Type 4 | Carbohydrate Metabolism Disorders | Reflex Epilepsy | Japanese Encephalitis | Spondylo-ocular Syndrome | Leukemia | Pilomatrix Carcinoma | Aneurysm, Thoracic Aortic | Fibromyalgia | Posterior Polar Cataract | Takayasu's Arteritis | Castleman Disease | Primary Carnitine Deficiency | Leri-Weill Dyschondrosteosis | Chudley-McCullough Syndrome | VACTERL Association | Spondylocostal Dysostosis | Hepatitis | Episodic Ataxia Type 1 | High Molecular Weight Kininogen Deficiency | Congenital Bile Acid Synthesis Defect | Peroxisomal Disorder | Congenital Disorders Of Glycosylation | Transthyretin-related Amyloidosis | Tyrosinemia Type 1 | Spinocerebellar Ataxia Type 5 | Congenital Fiber-type Disproportion Myopathy | Spinocerebellar Ataxia Type 40 | Congenital Ichthyosiform Erythroderma | Myofibromatosis | Cavitary Optic Disc Anomalies | Precocious Puberty | Orthostatic Intolerance | Glycogen Storage Disease Type 0 | Idiopathic Pulmonary Fibrosis | Retinal Diseases | Syncope | Nanophthalmos | Rett Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Duodenal Atresia | Pneumonia, Viral | Scleroderma | Borjeson-Forssman-Lehmann Syndrome | Hidradenitis Suppurativa | Communication Disorders | Meconium Ileus | Spinal Muscular Atrophy Type 2 | Combined Malonic And Methylmalonic Acidemia | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Heavy Chain Disease | Zimmermann-Laband Syndrome | Arthritis, Reactive | Dystonia | Gyrate Atrophy Of The Choroid And Retina | Tuberculosis | Stiff-man Syndrome | Hypolipoproteinemia | 3-methylcrotonyl-CoA Carboxylase Deficiency | Central Pain Syndrome | Peutz-Jeghers Syndrome | Lymphoma, Follicular | Tinea | Autonomic Nervous System Disorders | Blastomycosis | Primary Pigmented Nodular Adrenocortical Disease | Medulloblastoma | Paracoccidioidomycosis | Bladder Exstrophy | Birt-Hogg-Dube Syndrome | Disseminated Intravascular Coagulation | Heroin Dependence | Bronchiectasis | Necrobiosis Lipoidica | Acute Generalized Exanthematous Pustulosis | Growth Hormone Excess | Lamellar Ichthyosis | Thyroiditis, Autoimmune | Autosomal Recessive Congenital Ichthyosis | Gaucher Disease | Acromegaly | Non-small Cell Lung Cancer | Fowler's Syndrome | Distal Myopathy 2 | Vitamin B12 Deficiency | Left Ventricular Noncompaction | Noonan Syndrome | Robinow Syndrome | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Carbamoyl Phosphate Synthetase I Deficiency | X-linked Charcot-Marie-Tooth Disease | Fukuyama Congenital Muscular Dystrophy | Sarcoidosis | Lactose Intolerance | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Echinococcosis | Whipple's Disease | Cannabis Abuse | Hypertension, Renal | Rheumatic Heart Disease | Hypersomnia | Multiple Sclerosis, Relapsing-remitting | Glanzmann Thrombasthenia | Lichen Sclerosus | Fahr Disease | Dementia | Hypotrichosis Simplex | Situs Inversus | Optic Neuritis | Shock, Cardiogenic | Schaaf-Yang Syndrome | Nephronophthisis | Tetraplegia | Rhabdomyosarcoma, Embryonal | Constipation | Analgesia | Epidermolysis Bullosa | Schistosomiasis | Gray Platelet Syndrome | Adenomatoid Tumor | Microcephaly, Seizures, And Developmental Delay | Pemphigus Vulgaris | Hypodontia | Aceruloplasminemia | Spinocerebellar Ataxia Type 1 | Gastrointestinal Disorders | Lipodystrophy | Optic Neuropathy, Anterior Ischemic | Jalili Syndrome | Non-Langerhans Cell Histiocytosis | Patent Foramen Ovale | Filariasis | Raine Syndrome | Treacher Collins Syndrome | Gynecomastia | Autoimmune Hemolytic Anemia | Autism | Thrombocytopenia | Ectodermal Dysplasia | Amyotrophic Lateral Sclerosis, Juvenile | Myelomeningocele | Sarcoma | Hypertensive Retinopathy | Cerebral Amyloid Angiopathy | Giant Cell Arteritis | Microtia | Nephritis, Interstitial | Pachyonychia Congenita | Craniometaphyseal Dysplasia | Methylmalonic Aciduria And Homocystinuria, CblC Type | Lymphopenia | Episodic Ataxia | Venous Insufficiency | Pearson Syndrome | Lupus Erythematosus | Bietti Crystalline Dystrophy | Blue Rubber Bleb Nevus Syndrome | Familial Exudative Vitreoretinopathy | Rosacea | Benign Familial Infantile Seizures | Nemaline Myopathy | Creatine Deficiency Syndrome | Carcinoma In Situ | Pelizaeus-Merzbacher Disease | Carbonic Anhydrase VA Deficiency | Periodic Limb Movement Disorder | Melanocytic Nevus | Pendred Syndrome | Liebenberg Syndrome | Galactosialidosis | Dermatitis Herpetiformis | Behavioral Variant Of Frontotemporal Dementia | Hemophilia | Arthritis | Hypospadias | Vitreoretinal Degeneration, Snowflake Type | Migraine | Cataract | Rhabdomyosarcoma, Alveolar | Argininosuccinic Aciduria | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Dwarfism | Adrenoleukodystrophy, X-linked | Li-Fraumeni Syndrome | Tonsillitis | Ebstein Anomaly | Twin-to-twin Transfusion Syndrome | Chordoid Glioma | Glioblastoma | Hypogammaglobulinemia | Nance-Horan Syndrome | Usher Syndrome | Huntington's Disease-like 2 | Parkinson Disease 6, Autosomal Recessive Early-onset | Urticaria | Recurrent Respiratory Papillomatosis | Cornelia De Lange Syndrome | Cushing Syndrome | Colitis, Collagenous | Rothmund-Thomson Syndrome | Restrictive Dermopathy | Myeloid Leukemia | Stomatitis | Pancytopenia | Spermatocele | Yellow Fever | Glutaric Aciduria Type 2 | Hemoglobinopathies | Molybdenum Cofactor Deficiency | Trimethylaminuria | Skin Carcinoma | Chronic Inflammatory Demyelinating Polyneuropathy | Cartilage Disorders | Kearns-Sayre Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Cystitis | HANAC Syndrome | Osteonecrosis | Congenital Lipoid Adrenal Hyperplasia | Chromosome 16p11.2 Deletion Syndrome | Myoclonus-dystonia Syndrome | Hepatic Steatosis | Stromal Corneal Dystrophy | Enterocolitis, Necrotizing | Essential Fructosuria | Carcinoid Syndrome | Chylomicron Retention Disease | Cardiac Sarcoidosis | Combined Pituitary Hormone Deficiency | Progressive Familial Intrahepatic Cholestasis Type 2 | Cabezas Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Cholecystitis | Keratitis | McLeod Syndrome | Impetigo | Juvenile Xanthogranuloma | Schizencephaly | Adenoid Cystic Carcinoma | Kidney Stones | Cholera | Esophagitis | Diffuse Intrinsic Pontine Glioma | Persistent Truncus Arteriosus | Sarcoma, Ewing | Protein C Deficiency | T-cell Leukemia | Basal Cell Nevus Syndrome | Cyst | Progressive Familial Intrahepatic Cholestasis | Neuroendocrine Cancer | Spinocerebellar Ataxia Type 17 | Metachondromatosis | Cryptosporidiosis | Spinocerebellar Ataxia Type 42 | Genitopatellar Syndrome | Speech Disorders | Meningioma, Benign | Multiple Epiphyseal Dysplasia | Addison Disease | Multiple Sclerosis, Primary Progressive | Cold Agglutinin Disease | Ameloblastic Carcinoma | Spinocerebellar Ataxia Type 23 | Diabetes Type 1 | Stroke | Pineoblastoma | Axenfeld-Rieger Syndrome | Gastritis | Thrombophlebitis | Measles | Aromatic L-amino Acid Decarboxylase Deficiency | Distal Spinal Muscular Atrophy | Hypoglycemia | Dysferlinopathy | Cysticercosis | Eccrine Porocarcinoma | Familial Hyperaldosteronism | Mycosis Fungoides | Binge Eating Disorder | Burn-McKeown Syndrome | Spinocerebellar Ataxia Type 12 | Renpenning Syndrome | Cancer, Breast | Dysthymia | Feingold Syndrome