Disease

Eiken Syndrome

About the Disease
Eiken Syndrome, also known as eiken skeletal dysplasia, is related to osteochondrodysplasia and tooth ankylosis. An important gene associated with Eiken Syndrome is PTH1R (Parathyroid Hormone 1 Receptor), and among its related pathways/superpathways are Presynaptic function of Kainate receptors and Endochondral ossification. Affiliated tissues include bone and cortex, and related phenotypes are epiphyseal dysplasia and arthralgia

Common Targets
PTH1R

疾病靶点研报
Eiken Syndrome

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

Other Diseases

Cardiac Arrest | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Lymphedema-distichiasis Syndrome | Macular Degeneration | Antisocial Personality Disorder | Stroke, Hemorrhagic | Hermansky-Pudlak Syndrome | Ocular Surface Squamous Neoplasia | CHARGE Syndrome | Hyperparathyroidism, Secondary | Thin Basement Membrane Disease | Cutaneous Lupus Erythematosus | Spinocerebellar Ataxia Type 17 | Congenital Ichthyosiform Erythroderma | Obsessive-compulsive Disorder | Noonan Syndrome-like Disorder With Loose Anagen Hair | Cellulitis | Huntington's Disease | Autonomic Neuropathy | Iron Deficiency Anemia | Hamartoma | Desbuquois Syndrome | Personality Disorders | Muckle-Wells Syndrome | Gitelman Syndrome | Sarcoidosis, Pulmonary | Pseudohypoparathyroidism Type 1B | Birk-Barel Syndrome | Cervical Dystonia | Heroin Dependence | Dysplastic Nevus | Carcinoma, Transitional Cell | Exocrine Pancreatic Insufficiency | Postpartum Depression | Glycogen Storage Disease Type 0, Muscle | Nutrition Disorders | Nephritis, Interstitial | Vitamin B12 Deficiency | Trismus-pseudocamptodactyly Syndrome | Paraganglioma | Hemolytic Uremic Syndrome | Costello Syndrome | Hypospadias | Epiphyseal Chondrodysplasia, Miura Type | Muir-Torre Syndrome | Colorectal Adenoma | Carney Triad | Epidermolysis Bullosa | Pompe Disease | Angioedema, Hereditary | Cataplexy | Trichomegaly | Microcephaly, Seizures, And Developmental Delay | Tardive Dyskinesia | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Bladder Exstrophy | Cancer, Lung | Osteogenesis Imperfecta Type II | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Infantile Liver Failure Syndrome 1 | Nail-Patella Syndrome | Blastomycosis | Systemic Lupus Erythematosus | Liebenberg Syndrome | Waardenburg Syndrome Type 1 | Eczema | Central Pain Syndrome | Pierson Syndrome | Blau Syndrome | Dermatitis | Allergic Contact Dermatitis | Carbonic Anhydrase VA Deficiency | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Bronchitis | Urofacial Syndrome | Corneal Ulcer | Atrioventricular Septal Defect | Exostoses | Cocaine-Related Disorders | Leiomyosarcoma | Carcinoid Tumor | POEMS Syndrome | Neurofibroma | Cardiofaciocutaneous Syndrome | Veno-occlusive Disease | Aspergillosis | Hyperekplexia | Rhabdoid Tumor | Infectious Diarrhea | Lysosomal Acid Lipase Deficiency | Stuve-Wiedemann Syndrome | Myelofibrosis | Charcot-Marie-Tooth Disease, Type 1A | Mood Disorder | Aceruloplasminemia | Myositis, Focal | Autoimmune Polyendocrine Syndrome | Adenomyosis | Glycogen Storage Disease Type 4 | Acute Kidney Injury | Limb Girdle Muscular Dystrophy | Prader-Willi Syndrome | Phenylketonuria II | Mitochondrial Encephalomyopathy | Lactose Intolerance | Acral Lentiginous Melanoma | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Autosomal Recessive Spastic Paraplegia Type 75 | Congestive Heart Failure | Herpes Genitalis | Hyperuricemia | Hepatitis E | Cerebrotendinous Xanthomatosis | Keratosis, Seborrheic | Sezary Syndrome | Rhizomelic Chondrodysplasia Punctata | Osteonecrosis | Otosclerosis | GLUT1 Deficiency Syndrome | Obesity | Rolandic Epilepsy | Cluster Headache | Lateral Meningocele Syndrome | Goiter | Aspartylglycosaminuria | Homocystinuria | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Liver Diseases | Leukemia | Autosomal Recessive Bestrophinopathy | Exfoliative Dermatitis | Beare-Stevenson Syndrome | Spinocerebellar Ataxia Type 27 | Myelodysplasia | Monilethrix | Galloway-Mowat Syndrome | Muscular Dystrophy | Hypoplastic Left Heart Syndrome | Galactosemia | Pulmonary Veno-occlusive Disease | Congenital Dyserythropoietic Anemia Type 4 | Hyperkalemic Periodic Paralysis | Epidermolytic Hyperkeratosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Nephrotic Syndrome | Micro Syndrome | Thyroid Dyshormonogenesis | Analgesia | Kearns-Sayre Syndrome | Corneal Edema | Nephroblastoma | Epithelial-myoepithelial Carcinoma | Distal Spinal Muscular Atrophy | Cri-du-chat Syndrome | Enterocolitis, Necrotizing | Aldosterone Deficiency | Polycystic Kidney, Autosomal Dominant | Apert Syndrome | Blepharoconjunctivitis | Shprintzen-Goldberg Syndrome | Angiosarcoma Of The Breast | Stickler Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Bullous Pemphigoid | Porphyria Cutanea Tarda | Multiple Sclerosis, Relapsing-remitting | Intracerebral Hemorrhage | Hypertension, Renovascular | Fibrosarcoma | Evans Syndrome | Hyperlipidemia, Familial Combined | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Nephrocalcinosis | Cutis Laxa | Congenital Muscular Dystrophy | Hereditary Pyropoikilocytosis | Giant Axonal Neuropathy | Albinism | Hyperferritinemia-cataract Syndrome | Antenatal Bartter Syndrome Type 1 | Oligospermia | Lung Diseases | Zygomycosis | Hypertension, Pulmonary | Lissencephaly 2 | Spinocerebellar Ataxia Type 42 | Schnitzler Syndrome | Papillon-Lefevre Syndrome | Joubert Syndrome | Corneal Dystrophy And Perceptive Deafness | Seasonal Mood Disorder | Chordoid Glioma | Clouston Hidrotic Ectodermal Dysplasia | Carbohydrate Metabolism Disorders | Glaucoma, Congenital | Glycogen Storage Disease Type 6 | Alpha-1 Antitrypsin Deficiency | Liddle Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Thrombosis | Syndactyly | Myasthenia | Pachyonychia Congenita | Glutaric Aciduria Type 2 | Disseminated Superficial Actinic Porokeratosis | Loeys-Dietz Syndrome Type 4 | Papulopustular Rosacea | Cholelithiasis | Gingivitis | CREST Syndrome | Pseudohypoaldosteronism | Methylmalonic Acidemia | Chordoma | Spondylocarpotarsal Synostosis Syndrome | Reticular Dysgenesis | Otitis Media | Carcinoma, Signet Ring Cell | Dwarfism | Spinocerebellar Ataxia Type 14 | Orthostatic Intolerance | Rhabdomyosarcoma, Alveolar | Small Lymphocytic Lymphoma | Tyrosine Hydroxylase Deficiency | Metabolic Diseases | Holt-Oram Syndrome | Osteogenesis Imperfecta Type VI | Familial Pheochromocytoma-paraganglioma | Pancytopenia | Citrullinemia | Cyst | Asthma, Exercise-induced | Glomerulonephritis | Donnai-Barrow Syndrome | Primary Cutaneous Amyloidosis | Zellweger Syndrome | Adenomatoid Tumor | Reflex Epilepsy | Esophagitis | Sclerosteosis 2 | Neurofibromatosis Type 2 | Esophageal Motility Disorders | Hypereosinophilic Syndrome | Cherubism | Spinocerebellar Ataxia Type 10 | Meniere's Disease | Hemosiderosis | Anal Fissure | Autism Spectrum Disorders | Hypoparathyroidism | Optic Nerve Diseases | Episodic Ataxia Type 2 | Acrodermatitis Enteropathica | Odonto-onycho-dermal Dysplasia | Nemaline Myopathy | Leukemia-lymphoma, Adult T-cell | Wagner Disease | Agnathia-Otocephaly Complex | Ganglioglioma | Fucosidosis | Angina Pectoris | Autosomal Recessive Congenital Ichthyosis | SAPHO Syndrome | Seizures | Multisystemic Smooth Muscle Dysfunction Syndrome | Batten Disease | Frank-ter Haar Syndrome | Alkaptonuria | Xeroderma Pigmentosum | Glycogen Storage Disease Type 0 | Glycogen Storage Disease Type 3 | Porokeratosis | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Dental Caries | Ameloblastic Carcinoma | Mitochondrial Cytopathy | Lymphoma, B-cell | Pityriasis Rubra Pilaris | Tinea | Pure Autonomic Failure | Optic Neuropathy, Anterior Ischemic | Hypertelorism | Lichen Sclerosus | Arts Syndrome | Infantile Refsum Disease | Renal Tubular Dysgenesis | Cutaneous T-cell Lymphoma | Sialoadenitis | Silicosis | Binge Eating Disorder | Situs Inversus | Chronic Inflammatory Demyelinating Polyneuropathy | Pericarditis | Von Hippel-Lindau Disease | Brachial Plexus Neuropathy | HELLP Syndrome | Raynaud Phenomenon | Growth Hormone Excess | Hepatitis | Hyperlipidemia Type V | Gerodermia Osteodysplastica | Conjunctivitis | Xeroderma Pigmentosum Variant Type | Leber Hereditary Optic Neuropathy | Hypoproteinemia, Hypercatabolic | Focal Segmental Glomerulosclerosis | Craniopharyngioma | Thyroiditis, Autoimmune | Esthesioneuroblastoma | Bartsocas-Papas Syndrome | Schwartz-Jampel-Aberfeld Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Leri Pleonosteosis | Behcet's Disease | Arthritis | Geleophysic Dysplasia | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Autoimmune Disease | Ocular Hypertension | Achondrogenesis | Paroxysmal Nocturnal Hemoglobinuria | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Long QT Syndrome Type 3 | Angiomyolipoma | Transcobalamin Deficiency | Inflammatory Linear Verrucous Epidermal Nevus | Hereditary Hemorrhagic Telangiectasia | Hemochromatosis Type 2 | Liver Failure | Multiple Sclerosis | Rheumatic Heart Disease | Otopalatodigital Syndrome Type 2 | Patent Foramen Ovale | Adenylosuccinate Lyase Deficiency | Blue Rubber Bleb Nevus Syndrome | Androgen Insensitivity | Dengue Hemorrhagic Fever | Intracranial Hypertension | Duane Retraction Syndrome | Spinocerebellar Ataxia Type 3 | Spinocerebellar Ataxia Type 8 | Schwannomatosis | Hypotension, Orthostatic | Silver-Russell Syndrome | Chloridorrhea, Congenital | Hereditary Mixed Polyposis Syndrome | Dysthymia | Carey-Fineman-Ziter Syndrome | Rubeosis Iridis | Erythropoietic Protoporphyria | Ectrodactyly | Iron Overload | Infertility, Male | Adenosine Deaminase Deficiency | Acne | Sleep Disorder | Dyslexia | Hepatic Veno-occlusive Disease | Charcot-Marie-Tooth Disease Type 2D | Ichthyosis Bullosa Of Siemens | Hypercholesterolemia | GAPO Syndrome | Diabetes Gestational | Schaaf-Yang Syndrome | Thrombotic Microangiopathy | Sponastrime Dysplasia | Burn-McKeown Syndrome | Antithrombin III Deficiency | Olmsted Syndrome | Polycystic Ovary Syndrome | Hydrocephalus, Normal Pressure | Congenital Disorders Of Glycosylation Type II | Amelanotic Melanoma | Charcot-Marie-Tooth Disease Axonal Type 2N | Premenstrual Syndrome | Hemangioendothelioma | Hypersomnia | Kaposiform Hemangioendothelioma | Papillorenal Syndrome | Superficial Spreading Melanoma | Persistent Fetal Circulation | Combined Deficiency Of Factor V And Factor VIII | Spinocerebellar Ataxia Type 20 | Spinocerebellar Ataxia Type 5 | Chorea-acanthocytosis | Gastric Atrophy | Sensorineural Hearing Loss | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Cystitis, Interstitial | Idiopathic Pulmonary Fibrosis | Fibromyalgia | Lymphoma Lymphoblastic | Delayed Sleep Phase Syndrome | Hypogammaglobulinemia | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Diabetes Insipidus, Nephrogenic | Pulmonary Sclerosing Hemangioma | Chromosome 16p11.2 Deletion Syndrome | Hypermethioninemia | Synpolydactyly | 3-hydroxy-3-methylglutaric Aciduria