Disease

Zellweger Syndrome

About the Disease
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy, also known as christian syndrome, is related to nodular nonsuppurative panniculitis and panniculitis, and has symptoms including seizures An important gene associated with Mental Retardation, Skeletal Dysplasia, and Abducens Palsy is MRSD (Mental Retardation-Skeletal Dysplasia). The drugs Gastrointestinal Agents and Bile Acids and Salts have been mentioned in the context of this disorder. Affiliated tissues include bone, liver and heart, and related phenotypes are scoliosis and short stature

Common Targets
THRB | PEX26 | HSD17B4 | PEX16 | PEX1 | PEX6 | THRA | PEX3 | PEX10 | PEX12 | PEX13

疾病靶点研报
Zellweger Syndrome

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

Other Diseases

Hypertension | Congenital Diaphragmatic Hernia | Neurocysticercosis | Iron Metabolism Disorders | Metachondromatosis | Amyloidosis | Acanthosis Nigricans | Progressive Familial Intrahepatic Cholestasis | Spondylocarpotarsal Synostosis Syndrome | Rubinstein-Taybi Syndrome | Malonyl-CoA Decarboxylase Deficiency | Low Tension Glaucoma | Multicystic Renal Dysplasia | Retinal Dystrophy | Carcinoma, Merkel Cell | Anovulation | Autosomal Recessive Spastic Paraplegia Type 75 | Tonsillitis | Adenoma, Pituitary | Schizotypal Personality Disorder | Non-epidermolytic Palmoplantar Keratoderma | Precocious Puberty | Noonan Syndrome-like Disorder With Loose Anagen Hair | HIBCH Deficiency | Neurofibromatosis Type 1 | Kernicterus | Multiple Hamartoma Syndrome | Angina Pectoris | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Transcobalamin Deficiency | Hemangioma | Amish Infantile Epilepsy Syndrome | Lipoma | Autonomic Nervous System Disorders | Conduct Disorder | Polydactyly | Congenital Heart Block | Donnai-Barrow Syndrome | Melanoma, Malignant | McLeod Syndrome | Cone Dystrophy | Ichthyosis, X-linked | Hypermethioninemia | Esotropia | Cardiac Arrest | GAPO Syndrome | Influenza | CHOPS Syndrome | Polyarteritis Nodosa | Veno-occlusive Disease | Neuromuscular Disorders | Nanophthalmos | Scleritis | Vitelliform Macular Dystrophy | Conjunctivitis, Allergic | Glycogen Storage Disease Type 4 | Rett Syndrome | Sponastrime Dysplasia | Hyperandrogenemia | Congenital Absence Of Vas Deferens | Botulism | Pierson Syndrome | Adenomatoid Tumor | Reticular Dysgenesis | ACTH-independent Macronodular Adrenal Hyperplasia | Scapuloperoneal Spinal Muscular Atrophy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Cherubism | Richter's Syndrome | Lymphoma, Mantle Cell | Cyclic Vomiting Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Conjunctivitis | Peripheral T-cell Lymphoma | Heterotaxy | Overactive Bladder | Familial Isolated Hyperparathyroidism | Long QT Syndrome Type 1 | Angiodysplasia | Synovitis | NGLY1 Deficiency | Pure Red Cell Aplasia | Focal Facial Dermal Dysplasia | Feingold Syndrome | Neuroendocrine Cancer | Leber Hereditary Optic Neuropathy | Anal Fissure | Mucolipidosis | Episodic Ataxia | Barrett Esophagus | Glomerulonephritis | Oculocutaneous Albinism | Hypospadias | Malignant Fibrous Histiocytoma | WAGR Syndrome | Adenomyosis | Schnitzler Syndrome | Neuroectodermal Tumors, Primitive | Prurigo Nodularis | Congenital Hereditary Endothelial Dystrophy Type I | Christianson Syndrome | Pulmonary Alveolar Microlithiasis | Hyperinsulinemic Hypoglycemia | Spinocerebellar Ataxia Type 28 | Asthma, Nocturnal | Hypothyroidism | Pseudohermaphroditism | Gangliosidosis, GM1 | Lipid Metabolism Disorders | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Kaposi Sarcoma | Autonomic Neuropathy | Paronychia | Mevalonate Kinase Deficiency | Persistent Mullerian Duct Syndrome | Sertoli Cell-only Syndrome | Colon Adenoma | Renal-hepatic-pancreatic Dysplasia | Nance-Horan Syndrome | Hepatitis | Peters-plus Syndrome | Corneal Neovascularization | Encephalopathy | Congenital Generalized Lipodystrophy | Otosclerosis | Hypohidrotic Ectodermal Dysplasia | Tyrosinemia Type 1 | Dubin-Johnson Syndrome | Hyperbilirubinemia, Neonatal | Hemorrhoids | Wolcott-Rallison Syndrome | Hyperinsulinemia | Apraxia | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Persistent Hyperplastic Primary Vitreous | Macular Degeneration | Wolfram Syndrome | Chronic Thromboembolic Pulmonary Hypertension | Waardenburg Syndrome Type 4A | Dyslexia | Megaloblastic Anemia | Endometrial Hyperplasia | Eosinophilia | Primary Erythromelalgia | Leri-Weill Dyschondrosteosis | Maternally Inherited Diabetes And Deafness | Congenital Disorders Of Glycosylation Type II | X-linked Myotubular Myopathy | Glycogen Storage Disease Type 3 | Otitis Externa | Persistent Fetal Circulation | Diabetic Nephropathy | Chordoma | Babesiosis | Menetrier Disease | Fibrodysplasia Ossificans Progressiva | Necrobiosis Lipoidica | Pineoblastoma | HANAC Syndrome | Hydrocephalus, Normal Pressure | Diabetes Insipidus, Neurogenic | Spina Bifida | Spinocerebellar Ataxia Type 13 | Postaxial Polydactyly | Hypertelorism | Idiopathic Multicentric Castleman Disease | Congenital Afibrinogenemia | Leprosy | Ectrodactyly | Liebenberg Syndrome | Blastomycosis | Antenatal Bartter Syndrome Type 1 | Thalassemia | Renal Hypomagnesemia 3 | Pierpont Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Congenital Central Hypoventilation Syndrome | Gastric Atrophy | Hyperbilirubinemia | Long QT Syndrome Type 3 | Dementia, Vascular | Polycystic Kidney, Autosomal Recessive | Macular Corneal Dystrophy | Keloid | Hepatic Veno-occlusive Disease | Heart Septal Defects | Hyperparathyroidism, Primary | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Hypertension, Essential | Kawasaki Disease | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Microcephaly | Alagille Syndrome | Lymphedema-distichiasis Syndrome | Glaucomatocyclitic Crisis | Globozoospermia | Acne | Congenital Myopathy | Schwannomatosis | Stuttering | Liddle Syndrome | Glycogen Storage Disease Type 1 | Spinocerebellar Ataxia Type 42 | Sick Sinus Syndrome | Polymicrogyria | Familial Retinal Arterial Macroaneurysm | Peyronie's Disease | Cystinosis | Optic Neuritis | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Proctitis | Glucagonoma | Swine Influenza | Klippel-Feil Syndrome | Acrodysostosis | Diabetes Gestational | Adrenal Insufficiency | Graves Disease | Angioedema | Saethre-Chotzen Syndrome | Bare Lymphocyte Syndrome | Bone Giant Cell Tumor | Venous Insufficiency | Vitamin K Deficiency | Bartsocas-Papas Syndrome | Chronic Myelomonocytic Leukemia | Motion Sickness | Retinal Dystrophy, Early-onset Severe | Spondylo-ocular Syndrome | Hereditary Sensory Neuropathy Type 1 | Creatine Deficiency Syndrome | Prolymphocytic Leukemia | Retinitis Pigmentosa 3 | Crigler-Najjar Syndrome | Sleep Disorder | Myositis, Focal | Discoid Lupus Erythematosus | Adenoma, Pleomorphic | Antley-Bixler Syndrome | Mannosidase Deficiency Diseases | Leigh Syndrome | Ovarian Sex Cord-stromal Tumor | Demyelinating Diseases | Takotsubo Cardiomyopathy | Thanatophoric Dysplasia Type 1 | Hepatitis D | CREST Syndrome | Iron Deficiency Anemia | Menkes Disease | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Bone Marrow Necrosis | Primary Torsion Dystonia | Postpartum Depression | Chediak-Higashi Syndrome | Sickle Cell Anemia | Hypopituitarism | Gestational Trophoblastic Disease | Nephrocalcinosis | Inflammatory Joint Disease | Aldosteronism | Priapism | Sialidosis | Panniculitis | Retinitis | Clouston Hidrotic Ectodermal Dysplasia | B-cell Chronic Lymphocytic Leukemia | Epidermolysis Bullosa | X-linked Sideroblastic Anemia | Primary Progressive Aphasia | Barakat Syndrome | Cold Agglutinin Disease | Cholera | Persistent Truncus Arteriosus | Multiple Sclerosis, Primary Progressive | Myelitis | Celiac Disease | Aspergillosis | Hemorrhagic Disorders | Shprintzen-Goldberg Syndrome | Charcot-Marie-Tooth Disease Type 3 | Learning Disability | Heroin Dependence | Posterior Polar Cataract | Congenital Hypofibrinogenemia | Osteosarcoma | Acute Generalized Exanthematous Pustulosis | Asthma | Jawad Syndrome | Cervical Dystonia | Renal Tubular Acidosis | Erythropoietic Protoporphyria | Narcolepsy | Arteriovenous Malformations | Cutis Laxa | Congenital Bile Acid Synthesis Defect | Hypogammaglobulinemia | Acrodermatitis | Chronic Idiopathic Myelofibrosis | Restrictive Dermopathy | Erythema Nodosum | Multiple Epiphyseal Dysplasia | Porphyria, Acute Intermittent | Fahr Disease | Rotor Syndrome | Retinal Telangiectasia | Familial Male-limited Precocious Puberty | Spastic Paraplegia Type 7 | Withdrawal Syndrome | Bartter Syndrome | Stroke, Ischemic | Nemaline Myopathy 10 | Van Der Knaap Disease | Herpes Simplex Dermatitis | Hypervalinemia | Cold-induced Sweating Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Waardenburg Syndrome Type 4 | Glioma | Lymphedema | Chondrodysplasia Punctata 1, X-linked Recessive | Hepatitis, Autoimmune | Urofacial Syndrome | Iron Overload | Fetal Akinesia Deformation Sequence | Cancer, Bladder | Ependymoma | Ligneous Conjunctivitis | Joubert Syndrome 2 | Methylmalonic Acidemia | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Familial Cerebral Amyloid Angiopathy | Carey-Fineman-Ziter Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Muscle Wasting | Carcinoma, Signet Ring Cell | Facioscapulohumeral Muscular Dystrophy Type 2 | Exfoliative Dermatitis | Hereditary Coproporphyria | Specific Granule Deficiency | Basal Ganglia Disease | Osteopetrosis | Fanconi Anemia | Milk Allergy | Hyperostosis | Weill-Marchesani Syndrome | Ellis-Van Creveld Syndrome | Lentigo | Shwachman-Bodian-Diamond Syndrome | Hyperphenylalaninemia | Hydrolethalus Syndrome | Lipid Storage Diseases | Uterine Leiomyoma | Holt-Oram Syndrome | Dementia | Cluster Headache | Mumps | Autism | Angioimmunoblastic T-cell Lymphoma | Hypogonadism | Heart Block | Lathosterolosis | Familial Mediterranean Fever | Thanatophoric Dysplasia | Familial Exudative Vitreoretinopathy | Alpha-mannosidosis | Chronic Mucocutaneous Candidiasis | Autism Spectrum Disorders | Dengue Hemorrhagic Fever | Anorchia | Mohr-Tranebjaerg Syndrome | Atopy | Progressive External Ophthalmoplegia | Angiomyolipoma | Huntington's Disease-like 2 | Encephalitis | Methemoglobinemia | Adenosine Deaminase 2 Deficiency | Congenital Adrenal Hyperplasia | Erysipelas | Bietti Crystalline Dystrophy | Myocarditis | Microphthalmia | Fuchs Dystrophy | CEDNIK Syndrome | Ileitis | Adenylosuccinate Lyase Deficiency | Pulmonary Vein Stenosis | Insulinoma | Rheumatic Heart Disease | Ischemia | Thin Basement Membrane Disease | Cryptococcal Meningitis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Hypercalcemia | Muckle-Wells Syndrome | Filariasis | Basan Syndrome | Combined Malonic And Methylmalonic Acidemia | Cysticercosis