Disease

Pseudohermaphroditism

About the Disease
Pseudohermaphroditism, also known as indeterminate sex and pseudohermaphroditism, is related to leydig cell hypoplasia, type i and 17-beta hydroxysteroid dehydrogenase iii deficiency. An important gene associated with Pseudohermaphroditism is HSD17B3 (Hydroxysteroid 17-Beta Dehydrogenase 3), and among its related pathways/superpathways are Metabolism and Metabolism of steroids. Affiliated tissues include testis, ovary and adrenal cortex, and related phenotypes are Decreased caspase 3/7 activity and growth/size/body region

Common Targets
CYP11A1 | ACADM | HSD17B3

疾病靶点研报
Pseudohermaphroditism

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

Other Diseases

Progressive External Ophthalmoplegia | Glutathione Synthetase Deficiency | Congenital Aniridia | Lymphoma Lymphoblastic | Acanthosis Nigricans | Leiomyosarcoma | Hyperammonemia | Loeys-Dietz Syndrome | Crimean-Congo Hemorrhagic Fever | Hypertension | Vitiligo | Renal Tubular Dysgenesis | Hemolytic Anemia | Niemann-Pick Disease | Pyloric Stenosis, Infantile Hypertrophic | Pycnodysostosis | Leishmaniasis, Visceral | Primary Hyperoxaluria Type 3 | Progressive Familial Intrahepatic Cholestasis Type 2 | Diabetes Mellitus, Transient Neonatal | Idiopathic Multicentric Castleman Disease | Cerebellar Ataxia, Cayman Type | Adrenal Insufficiency | Leukemia | Polymicrogyria | Juvenile Polyposis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Pericarditis | Carcinoid Tumor | Periventricular Nodular Heterotopia | KBG Syndrome | ICF Syndrome | Avellino Corneal Dystrophy | Sarcoma, Ewing | Blomstrand Osteochondrodysplasia | Li-Fraumeni Syndrome | Tendinitis | Pleurisy | Hereditary Spastic Paraplegia | Portal Vein Thrombosis | Periodic Limb Movement Disorder | Babesiosis | Nephrocalcinosis | Psoriasis | Cutis Laxa | Familial Thoracic Aortic Aneurysm | Long QT Syndrome Type 2 | Rubinstein-Taybi Syndrome | Carcinoma, Squamous Cell | Wieacker-Wolff Syndrome | Common Variable Immunodeficiency | Cholangitis | Reticular Dysgenesis | Pontocerebellar Hypoplasia Type 2 | Polycystic Ovary Syndrome | Fibromuscular Dysplasia | Brachial Plexus Neuropathy | Ovarian Sex Cord-stromal Tumor | Angiosarcoma Of The Breast | Microvillus Inclusion Disease | Hereditary Inclusion Body Myopathy | Waldenstrom Macroglobulinemia | Acute Kidney Injury | Encephalitis | Neurofibromatosis-Noonan Syndrome | Alopecia Areata | Costello Syndrome | Keratoacanthoma | Asplenia | Polyomavirus Nephropathy | Liver Failure | Whipple's Disease | Headache | Tumoral Calcinosis | Disseminated Superficial Actinic Porokeratosis | Spinocerebellar Ataxia Type 15 | Aldosterone Deficiency | Spinocerebellar Ataxia Type 3 | Anorchia | Maternally Inherited Diabetes And Deafness | IgA Nephropathy | Aspartylglycosaminuria | Hypertensive Retinopathy | Peutz-Jeghers Syndrome | Tetraplegia | Adenomatoid Tumor | Congenital Adrenal Hyperplasia | Riboflavin Transporter Deficiency Neuronopathy | Mixed Connective Tissue Disease | Chondroma | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Smith-Lemli-Opitz Syndrome | Mevalonate Kinase Deficiency | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Histiocytic Sarcoma | Apparent Mineralocorticoid Excess Syndrome | Salla Disease | Diabetic Nephropathy | Chondrodysplasia Punctata 2, X-linked Dominant | Granular Corneal Dystrophy Type 1 | Thrombotic Microangiopathy | Ventricular Septal Defect | Sporadic Hemiplegic Migraine | Epidermolytic Palmoplantar Keratoderma | Vitreoretinopathy, Proliferative | Familial Advanced Sleep Phase Syndrome | Wilson's Disease | Menetrier Disease | Spondylocarpotarsal Synostosis Syndrome | Anthrax | Lymphopenia | Spinocerebellar Ataxia Type 23 | Hyper IgE Syndrome | Blastoma, Pleuropulmonary | Poirier-Bienvenu Neurodevelopmental Syndrome | Acrodermatitis | Glycogen Storage Disease Type 5 | Schindler Disease | Neurofibromatosis | Central Retinal Artery Occlusion | Cole-Carpenter Syndrome | Dermatitis Herpetiformis | Joubert Syndrome | Spinal Cord Diseases | Cat Eye Syndrome | 3C Syndrome | Optic Neuritis | Diabetic Macular Edema | Kaposiform Hemangioendothelioma | Granuloma Annulare | Lipid Metabolism Disorders | Tyrosinemia Type 2 | Cornelia De Lange Syndrome | Congenital Dyserythropoietic Anemia Type 1 | NGLY1 Deficiency | Arteriosclerosis | Multiple Sclerosis, Primary Progressive | Gout | Osteopetrosis | Empyema | Uremic Pruritus | Meniere's Disease | Spinocerebellar Ataxia Type 1 | Calcium Pyrophosphate Deposition Disease | Alkaptonuria | Congenital Afibrinogenemia | Hepatic Veno-occlusive Disease | Pancreatitis | Rett Syndrome | REM Sleep Behavior Disorder | Gastroenteritis, Eosinophilic | Spinocerebellar Ataxia Type 6 | Congenital Hemolytic Anemia | Thanatophoric Dysplasia | Primary Erythromelalgia | Borderline Personality Disorder | Swine Influenza | Epidermolysis Bullosa Dystrophica | Hyperlipidemia | Herpes Simplex Dermatitis | Follicular Dendritic Cell Sarcoma | Hemorrhage | Amenorrhea | Pyoderma Gangrenosum | Benign Hereditary Chorea | Congenital Heart Defects | Chondrodysplasia Punctata | Filariasis | Sensory Neuropathy | Glaucomatocyclitic Crisis | Hoyeraal-Hreidarsson Syndrome | Cholera | Carcinoma, Merkel Cell | Epiphyseal Chondrodysplasia, Miura Type | Spinocerebellar Ataxia Type 13 | Cancer, Bladder | Open-angle Glaucoma | Spitzoid Melanoma | Bacterial Meningitis | Omenn Syndrome | Carney Triad | DNA Ligase IV Deficiency | Glioblastoma Multiforme | Kohlschutter-Tonz Syndrome | Cutaneous Lupus Erythematosus | Ureteropelvic Junction Obstruction | Syphilis | Phenylketonuria | Stomatitis | Chronic Inflammatory Demyelinating Polyneuropathy | Choroiditis | Hemangioblastoma | Pearson Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Tuberculous Meningitis | Tibial Muscular Dystrophy | Osteogenesis Imperfecta Type I | Facioscapulohumeral Muscular Dystrophy | Delirium | Astrocytoma | Distal Spinal Muscular Atrophy | Creatine Deficiency Syndrome Due To AGAT Deficiency | Hypertriglyceridemia | Down Syndrome | Pyruvate Carboxylase Deficiency Disease | Congenital Hereditary Endothelial Dystrophy Type II | Presbyopia | Pemphigoid | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Erythropoietic Protoporphyria | Cenani-Lenz Syndactyly Syndrome | Carcinoma In Situ | Diabetes Type 1 | Molybdenum Cofactor Deficiency | Situs Inversus | Amelanotic Melanoma | Nager Acrofacial Dysostosis | Cataract | Mycosis Fungoides | Polycystic Kidney, Autosomal Dominant | Benign Recurrent Intrahepatic Cholestasis 1 | Epidermal Nevus Syndrome | Prune Belly Syndrome | Urea Cycle Disorder | Hypocalcemia | Behcet's Disease | Harlequin Ichthyosis | Acute Motor Axonal Neuropathy | Alcoholism | Varicocele | Fahr Disease | Alpha-1 Antitrypsin Deficiency | Campomelic Dysplasia | Ependymoma | Chronic Myeloid Leukemia | Persistent Hyperplastic Primary Vitreous | Hyperuricemic Nephropathy, Familial Juvenile | Methemoglobinemia | Raine Syndrome | Galactosemia | Hypertrophy | Epicondylitis | Odonto-onycho-dermal Dysplasia | Oculocutaneous Albinism Type 1 | D-2-Hydroxyglutaric Aciduria | Epidermolytic Ichthyosis, Annular | Oligospermia | Primary Aldosteronism | Focal Cortical Dysplasia Type 2 | Blepharoconjunctivitis | Adenomyosis | Spinocerebellar Ataxia Type 27 | Osteogenesis Imperfecta Type IV | Neurocutaneous Melanocytosis | Localized Scleroderma | GATA2 Deficiency | Hypokalemia | Glanzmann Thrombasthenia | Porphyria, Variegate | Torticollis | Kernicterus | Hydronephrosis | Autism | Focal Dermal Hypoplasia | Basal Ganglia Cerebrovascular Disease | Achondrogenesis | Ichthyosis Bullosa Of Siemens | Spastic Paraplegia Type 7 | Priapism | DEND Syndrome | Sialoadenitis | Esophageal Carcinoma | Infertility | Recurrent Respiratory Papillomatosis | Jacobsen Syndrome | Tietze Syndrome | T-cell Chronic Lymphocytic Leukemia | Silicosis | Multiple Sclerosis, Secondary Progressive | Agranulocytosis | Anuria | Gastritis, Atrophic | Snyder-Robinson Syndrome | Osteogenesis Imperfecta Type II | Keratosis, Seborrheic | Hemophagocytic Lymphohistiocytosis | Intestinal Tuberculosis | Aphasia | Primrose Syndrome | Heavy Chain Disease | Cancer, Prostate | Blau Syndrome | Trichothiodystrophy | Low Tension Glaucoma | Neuromyotonia | Adenoma, Pituitary | H Syndrome | Primary Ovarian Insufficiency | Autoimmune Polyendocrinopathy Syndrome Type I | Cardiomyopathy, Restrictive | Arthritis, Gouty | Polyneuropathy | Multisystemic Smooth Muscle Dysfunction Syndrome | Twin-to-twin Transfusion Syndrome | Glycogen Storage Disease Type 1b | Porphyria, Acute Intermittent | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Alpha-thalassemia Myelodysplasia Syndrome | Intestinal Obstruction | Thrombocytopenia | Myoclonic Atonic Epilepsy | Charcot-Marie-Tooth Disease Type 2D | Hyperostosis | Sarcoma, Endometrial Stromal | Neuromuscular Disorders | Nemaline Myopathy | Bronchiolitis | Pneumothorax | Glutaric Aciduria Type 3 | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Osteonecrosis Of The Jaw | Sertoli Cell-only Syndrome | Hypodontia | Reye Syndrome | Endometriosis | Gastrointestinal Disorders | Acute Lung Injury | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Tularemia | Ectrodactyly | Anti-NMDA Receptor Encephalitis | Rift Valley Fever | McCune-Albright Syndrome | Cushing Syndrome | 5-oxoprolinase Deficiency | Arthrogryposis | Necrotizing Autoimmune Myopathy | Aldosterone Synthase Deficiency | High Molecular Weight Kininogen Deficiency | GLUT1 Deficiency Syndrome | Infantile Refsum Disease | Charcot-Marie-Tooth Disease Type 4B1 | Antley-Bixler Syndrome | Alazami Syndrome | Panniculitis | Nicotine Dependence | Angioimmunoblastic T-cell Lymphoma | Adrenomyeloneuropathy | Mastitis | 3-M Syndrome | Glucagonoma | Huntington's Disease-like 2 | Congenital Myopathy | Spinal Muscular Atrophy Type 2 | Acral Lentiginous Melanoma | Epidermolysis Bullosa Acquisita | Autoimmune Polyendocrine Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Multiple Epiphyseal Dysplasia | Pemphigus Vulgaris | Left Ventricular Noncompaction | Thalassemia, Beta | Stiff-man Syndrome | Perivascular Epithelioid Cell Tumor | Usher Syndrome Type II | Retinitis | Encephalocele | Carney-Stratakis Syndrome | Congenital Dyserythropoietic Anemia Type 4 | Congenital Bile Acid Synthesis Defect | Vertigo | Poretti-Boltshauser Syndrome | Osteochondroma | Orthostatic Intolerance | Rhizomelic Chondrodysplasia Punctata | Heterotopic Ossification | Ophthalmoplegia | Hermansky-Pudlak Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Ischemia | Phenylketonuria II | Ileitis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Thromboembolism | Proteasome-associated Autoinflammatory Syndrome 2 | Cholangiocarcinoma | Autonomic Nervous System Disorders | Cleidocranial Dysplasia | Diabetes Insipidus | Hepatitis D | Sclerocornea | Ghosal Syndrome | Trigonocephaly | Paroxysmal Kinesigenic Dyskinesia | Epidermolysis Bullosa | Pyelonephritis | Richter's Syndrome | Wolfram Syndrome 2 | Marshall-Smith Syndrome | Hypersensitivity Pneumonitis