Disease

Kallmann Syndrome

About the Disease
Hypogonadotropic Hypogonadism 1 with or Without Anosmia, also known as dysplasia olfactogenitalis of de morsier, is related to hypogonadotropic hypogonadism 23 with or without anosmia and normosmic congenital hypogonadotropic hypogonadism. An important gene associated with Hypogonadotropic Hypogonadism 1 with or Without Anosmia is ANOS1 (Anosmin 1), and among its related pathways/superpathways are Negative regulation of FGFR1 signaling and Signaling by FGFR2. The drugs Zinc cation and Follitropin have been mentioned in the context of this disorder. Affiliated tissues include pituitary, breast and eye, and related phenotypes are facial asymmetry and micropenis

Common Targets
HESX1 | SEMA7A | PTCH1 | GLI3 | IGFALS | PROK2 | CHD7 | IL17RD | NRP2 | GNRH1 | FEZF1 | PLXNA1 | PNPLA6 | FGF8 | NRP1 | EBF2 | GNRHR | PTPN11 | CCDC141 | ANOS1 | POLR3B | DMXL2 | SEMA3A | SOX10 | WDR11 | POLR3A | KISS1R | PROKR2 | AXL | FGFR1

疾病靶点研报
Kallmann Syndrome

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

Other Diseases

Spondylometaphyseal Dysplasia | Osteogenesis Imperfecta Type V | Oguchi Disease-2 | Hypodontia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Peeling Skin Syndrome, Acral Type | AIDS | Pseudohypoparathyroidism Type 1C | Blepharoconjunctivitis | Nemaline Myopathy 10 | Celiac Disease | Pure Autonomic Failure | Chronic Lymphocytic Leukemia | Osteonecrosis Of The Jaw | Wagner Disease | Osteosclerosis | Tetanus | Metachromatic Leukodystrophy | Congenital Dyserythropoietic Anemia Type 1 | Ventricular Septal Defect | Early Infantile Epileptic Encephalopathy 1 | Lassa Fever | Tendinopathy | Glycogen Storage Disease | Exfoliative Dermatitis | Preaxial Polydactyly | Sezary Syndrome | Keratopathy | Periodic Limb Movement Disorder | Spinal Muscular Atrophy Type 2 | Contact Dermatitis | Progressive Encephalopathy-optic Atrophy Syndrome | Esophagitis | Porphyria | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Glioblastoma | Primary Lateral Sclerosis | Hyperkalemic Periodic Paralysis | Milk Allergy | Osteoporosis-pseudoglioma Syndrome | Relapsing Polychondritis | Temtamy Preaxial Brachydactyly Syndrome | Trichorhinophalangeal Syndrome | N-acetylglutamate Synthase Deficiency | Glaucoma, Congenital | Osteogenesis Imperfecta Type II | Gnathodiaphyseal Dysplasia | Methylmalonic Aciduria And Homocystinuria, CblC Type | Ureteropelvic Junction Obstruction | Alveolar Capillary Dysplasia | Myotonia | Waardenburg Syndrome Type 2A | Rhabdoid Tumor | Brachydactyly | Congenital Bilateral Absence Of Vas Deferens | Spinocerebellar Ataxia Type 28 | Anovulation | Hyperthyroidism | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Hyperparathyroidism-jaw Tumor Syndrome | Ligneous Conjunctivitis | Progressive Myoclonic Epilepsy | Chromosome 17q21.31 Deletion Syndrome | Congenital Heart Block | Charcot-Marie-Tooth Disease Type 4 | Thromboembolism | Autosomal Recessive Bestrophinopathy | Cutis Laxa | Thyroiditis, Autoimmune | Autonomic Nervous System Disorders | Lymphangioma | Plasma Cell Dyscrasia | Lissencephaly 2 | Pendred Syndrome | Pompe Disease | Familial Thoracic Aortic Aneurysm | Cataplexy | Down Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Conjunctivitis, Allergic | Keratitis-ichthyosis-deafness Syndrome | Micro Syndrome | Congenital Lipoid Adrenal Hyperplasia | Globozoospermia | Ganglioneuroma | Benign Familial Pemphigus | Specific Granule Deficiency | Acute Coronary Syndrome | Birk-Barel Syndrome | Proctitis | GAPO Syndrome | Schizophrenia, Paranoid | Glaucoma | Hypoproteinemia, Hypercatabolic | Progressive External Ophthalmoplegia | Leber Hereditary Optic Neuropathy | Stargardt Disease | Lamellar Ichthyosis | Acute Chest Syndrome | Osteochondrosis | Noonan Syndrome | Sleep Apnea | Perivascular Epithelioid Cell Tumor | Language Disorders | Congenital Dysfibrinogenemia | Raine Syndrome | Blepharitis | Alopecia Totalis | Hypereosinophilic Syndrome | Heavy Chain Disease | Kernicterus | Atrioventricular Septal Defect | Chronic Periodontitis | Glaucomatocyclitic Crisis | Methemoglobinemia Type IV | Hyperinsulinism-hyperammonemia Syndrome | Hemorrhage | Cardiomyopathy, Hypertrophic | Combined Pituitary Hormone Deficiency | Tardive Dyskinesia | Smith-Kingsmore Syndrome | Essential Fructosuria | Peripheral Neuropathy | Amelogenesis Imperfecta | Pneumonia, Mycoplasma | Lyme Disease | Porencephaly | Progressive Familial Intrahepatic Cholestasis Type 3 | Scleroderma | Spinocerebellar Ataxia Type 5 | Cerebellofaciodental Syndrome | Presbyopia | Short-chain Acyl-CoA Dehydrogenase Deficiency | Atelosteogenesis Type 1 | Chudley-McCullough Syndrome | Congenital Central Hypoventilation Syndrome | Early Infantile Epileptic Encephalopathy | Hemangioblastoma | Lentigo | Trismus-pseudocamptodactyly Syndrome | Hypothalamic Obesity | Cyst | Epidermolysis Bullosa Simplex, Generalized | Ileitis | Epidermodysplasia Verruciformis | Congenital Nystagmus | Diabetes Insipidus | Kabuki Syndrome 2 | Cholecystitis | Pearson Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Niemann-Pick Disease, Type A | Aceruloplasminemia | Cholangiocarcinoma | Osteomyelitis | Succinic Semialdehyde Dehydrogenase Deficiency | Congenital Disorders Of Glycosylation | Hyperbilirubinemia | Hereditary Mixed Polyposis Syndrome | Rash | Esophageal Carcinoma | Harlequin Ichthyosis | Erythromelalgia | Purpura | Renal Hypomagnesemia 3 | Glutaric Aciduria Type 2 | Azoospermia | Anosmia, Congenital | Glycogen Storage Disease Type 0 | Weill-Marchesani Syndrome | Chorioretinitis | Dysfibrinogenemia | Costello Syndrome | Nicotine Dependence | Nephroblastoma | Leishmaniasis, Visceral | Coenzyme Q10 Deficiency | Non-Langerhans Cell Histiocytosis | Bone Marrow Necrosis | Paget's Disease Of The Breast | Pontocerebellar Hypoplasia Type 2 | Multiple Myeloma | Parkinson's Disease | Fanconi Anemia | Goiter | Poikiloderma With Neutropenia | Hyperglycemia | Adenomyosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Papilledema | Brugada Syndrome 1 | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Homocystinuria | NDH Syndrome | Megaloblastic Anemia | Facioscapulohumeral Muscular Dystrophy | Dowling-Degos Disease | 3-methylglutaconic Aciduria Type IV | Sertoli Cell-only Syndrome | Progressive Familial Intrahepatic Cholestasis | Neuronal Ceroid Lipofuscinosis | Alexander Disease | Neurofibroma | Personality Disorders | Multiple Epiphyseal Dysplasia | Yellow Fever | Duane Retraction Syndrome | Bacterial Meningitis | Lennox-Gastaut Syndrome | Stickler Syndrome | Jaundice, Obstructive | Cancer, Breast | Klippel-Feil Syndrome | Lymphoproliferative Disease, X-linked | L-2-Hydroxyglutaric Aciduria | Pemphigus Vulgaris | Sensory Neuropathy | Chondroma | Schizoaffective Disorder | Glycogen Storage Disease Type 1b | Cholestasis | Choroideremia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Osteonecrosis | Dyskeratosis Congenita | McCune-Albright Syndrome | Primrose Syndrome | Cleidocranial Dysplasia | HELLP Syndrome | Dysmorphophobia | Schnyder Crystalline Corneal Dystrophy | Gastroenteritis | Schizencephaly | Keratoconus | Tularemia | Nager Acrofacial Dysostosis | Acute Leukemia | Autism | Multiple Sclerosis, Primary Progressive | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Arteriovenous Malformations | Cluster Headache | Myocardial Infarction | Diabetes Type 1 | Waardenburg Syndrome Type 2E | X-linked Charcot-Marie-Tooth Disease | Alzheimer Disease, Late Onset | Meckel-Gruber Syndrome | HANAC Syndrome | Aldosterone Deficiency | Histiocytic Sarcoma | Craniopharyngioma | Spasticity | Hereditary Sensory Neuropathy Type 1 | Otopalatodigital Syndrome Type 2 | Von Willebrand Disease | CHARGE Syndrome | Cancer, Lung | Smith-Lemli-Opitz Syndrome | Oligoastrocytoma | Spondylocarpotarsal Synostosis Syndrome | Choriocarcinoma | Hydrocephalus, Normal Pressure | Takotsubo Cardiomyopathy | Schindler Disease | Spinocerebellar Ataxia Type 31 | Lymphedema | Familial Retinal Arterial Macroaneurysm | Pantothenate Kinase-associated Neurodegeneration | Cri-du-chat Syndrome | Pseudoachondroplasia | Cholelithiasis | Aspergillosis | Neuroblastoma | Neuroendocrine Cancer | Nephronophthisis | Eiken Syndrome | Exostoses | Prurigo Nodularis | Urea Cycle Disorder | Chromosome 9q34.3 Deletion Syndrome | Anorexia Nervosa | Fascioliasis | Macular Corneal Dystrophy Type 1 | Huntington's Disease-like 2 | Hereditary Multiple Exostoses | Hyperekplexia | Amyloidosis | Photosensitivity | Astrocytoma, Anaplastic | Uveitis, Anterior | Menetrier Disease | Diabetic Neuropathy | Leukocyte Adhesion Deficiency Type 1 | Intermittent Explosive Disorder | Congenital Mirror Movements | Syncope | Melanoma, Malignant | FG Syndrome | Optic Atrophy 2 | Coffin-Siris Syndrome | Delirium | Stroke, Ischemic | Combined Deficiency Of Factor V And Factor VIII | Pterygium | Endocarditis | Polycystic Ovary Syndrome | Leprosy | Schwannoma | Fabry's Disease | Meningitis | B-cell Prolymphocytic Leukemia | Bronchitis, Chronic | Focal Cortical Dysplasia Type 2 | Carney-Stratakis Syndrome | Hashimoto Thyroiditis | Retinoschisis | Osteopathia Striata With Cranial Sclerosis | Skin Carcinoma | Spondylolisthesis | Pleomorphic Xanthoastrocytoma | Blastomycosis | Glucagonoma | Hyperferritinemia-cataract Syndrome | Myotonic Disorders | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Parkinsonism | Leukemia | Schamberg Disease | Corneal Neovascularization | Currarino Syndrome | Herpes Simplex Dermatitis | Pathological Gambling | Amyotrophic Lateral Sclerosis, Juvenile | Neurofibromatosis Type 1 | Conduct Disorder | Crigler-Najjar Syndrome | Keratosis, Actinic | Prolymphocytic Leukemia | Adenoma, Pleomorphic | Alopecia | Cabezas Syndrome | Meniere's Disease | Rheumatoid Arthritis | Incontinentia Pigmenti | Inflammatory Bowel Disease | Cerebellar Ataxia, Cayman Type | Autonomic Neuropathy | Feingold Syndrome | Waardenburg Syndrome Type 4 | Hepatic Adenomatosis | Walker-Warburg Syndrome | Reticular Dysgenesis | Malignant Fibrous Histiocytoma | Osteopetrosis | Androgen Insensitivity | Congenital Muscular Dystrophy | Strabismus | Otitis Media | Lesch-Nyhan Syndrome | Hemangioma | Ehlers-Danlos Syndrome | Nemaline Myopathy 8 | Juvenile Xanthogranuloma | Chromosome 16p11.2 Deletion Syndrome | Hyperlipidemia Type V | Hepatopulmonary Syndrome | Leukocyte Adhesion Deficiency | Familial Pheochromocytoma-paraganglioma | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Cervicitis | Familial Hypertrophic Cardiomyopathy | Skin Fragility-woolly Hair Syndrome | Exocrine Pancreatic Insufficiency | B-cell Chronic Lymphocytic Leukemia | Mandibuloacral Dysplasia With Type A Lipodystrophy | Polycythemia | Premature Ejaculation | Epidermolysis Bullosa | Potocki-Shaffer Syndrome | Antisynthetase Syndrome | Colon Adenoma | Dubin-Johnson Syndrome | Glioblastoma Multiforme | Diabetic Nephropathy | Ichthyosis Bullosa Of Siemens | Extramammary Paget's Disease | Macular Corneal Dystrophy | Swine Influenza | Crisponi Syndrome | CREST Syndrome | Carcinoma In Situ | Acute Motor Axonal Neuropathy | Hypertriglyceridemia | Galactosemia | Anti-glomerular Basement Membrane Disease | Myasthenia | Transcobalamin Deficiency | Colitis, Collagenous