Disease

Cabezas Syndrome

About the Disease
Intellectual Developmental Disorder, X-Linked, Syndromic, Cabezas Type, also known as cabezas syndrome, is related to syndromic x-linked intellectual disability cabezas type and alacrima, achalasia, and mental retardation syndrome, and has symptoms including tremor and gait ataxia. An important gene associated with Intellectual Developmental Disorder, X-Linked, Syndromic, Cabezas Type is CUL4B (Cullin 4B). Affiliated tissues include testes, skin and brain, and related phenotypes are short neck and inguinal hernia

Common Targets
CUL4B

疾病靶点研报
Cabezas Syndrome

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

Other Diseases

Congenital Afibrinogenemia | Vitreoretinopathy, Proliferative | Bronchitis | Schistosomiasis | Supravalvular Aortic Stenosis | Lamellar Ichthyosis | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Congenital Dysfibrinogenemia | Epidermolysis Bullosa Simplex | Intracerebral Hemorrhage | Hyperoxaluria | Achromatopsia | Otitis Externa | Hemimegalencephaly | Carey-Fineman-Ziter Syndrome | Portal Vein Thrombosis | Sleep Apnea, Central | Autism Spectrum Disorders | Seasonal Mood Disorder | Spinocerebellar Ataxia Type 1 | Jawad Syndrome | Obesity | Fibrodysplasia Ossificans Progressiva | Hepatitis A | Hepatopulmonary Syndrome | Stroke, Ischemic | Hypertension, Portal | Arterial Tortuosity Syndrome | Platelet Disorders | Encephalopathy | Familial Retinal Arterial Macroaneurysm | Sarcoma, Alveolar Soft Part | Hartnup Disease | Encephalopathy, Hepatic | Nemaline Myopathy | Achondrogenesis | Angioedema, Acquired | Tinea | Camptocormia | Tardive Dyskinesia | Pseudohypoparathyroidism Type 1A | Meesmann Corneal Dystrophy | Priapism | Antisocial Personality Disorder | Pantothenate Kinase-associated Neurodegeneration | Neurotoxicity | Charcot-Marie-Tooth Disease, Type 1A | Porphyria | Hypermetropia | Cellulitis | Tenosynovial Giant Cell Tumor | Chronic Beryllium Disease | Acute Generalized Exanthematous Pustulosis | Hereditary Multiple Exostoses | Cerebrotendinous Xanthomatosis | Chronic Granulomatous Disease | Schizencephaly | Impulse Control Disorder | Azoospermia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Hepatitis, Alcoholic | Colitis, Collagenous | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Purpura, Thrombotic Thrombocytopenic | Meniere's Disease | Neuromyotonia | Primary Pigmented Nodular Adrenocortical Disease | Paget's Disease Of The Breast | Intestinal Hypomagnesemia 1 | Anti-NMDA Receptor Encephalitis | Gangliosidosis | Hairy Cell Leukemia | Spastic Paraplegia Type 7 | 3-methylglutaconic Aciduria | Crigler-Najjar Syndrome | Epidermolysis Bullosa Simplex, Localized | Arthritis, Gouty | Cardiac Sarcoidosis | Aplastic Anemia | Progressive Encephalopathy-optic Atrophy Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Hypersensitivity Pneumonitis | Congenital Myopathy | Pseudohypoparathyroidism Type 1B | Diabetic Neuropathy | Iron Metabolism Disorders | Gout | Paternal Uniparental Disomy Of Chromosome 14 | Lattice Corneal Dystrophy | X-linked Myotubular Myopathy | Blepharospasm | Ophthalmoplegia | Milk Allergy | Corticobasal Syndrome | Postpartum Depression | Glutaric Aciduria Type 3 | Thrombosis | Congenital Stationary Night Blindness | Polycystic Liver | Plasma Cell Dyscrasia | Thalassemia | Glutaric Aciduria Type 2 | Glomerulonephritis | Primary Ovarian Insufficiency | Brugada Syndrome 1 | Leukodystrophies | Hepatitis B, Chronic | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Spitz Nevus | Communication Disorders | Angioedema | Aicardi-Goutieres Syndrome | Lupus Erythematosus | Tricho-hepato-enteric Syndrome | Panuveitis | Erythrokeratodermia Variabilis | Precocious Puberty | Stargardt Disease | Heterotopic Ossification | Depression | Lipid Storage Myopathy | Creatine Deficiency Syndrome | Multiple Epiphyseal Dysplasia | Blepharo-cheilo-odontic Syndrome | Osteomalacia | Aspartylglycosaminuria | Cryoglobulinemia | Thalassemia, Beta | Diabetes Insipidus, Nephrogenic | Vertigo | Diastrophic Dysplasia | Sporadic Inclusion Body Myositis | Inflammatory Linear Verrucous Epidermal Nevus | Analgesia | Proteus Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Cutaneous Mastocytosis | Hypotrichosis | Venous Insufficiency | Beare-Stevenson Syndrome | PHARC Syndrome | Schwannoma | Epicondylitis | Metaphyseal Chondrodysplasia, Schmid Type | Ichthyosis Hystrix, Curth-Macklin Type | Atelosteogenesis Type 2 | Hypopigmentation | B-cell Prolymphocytic Leukemia | Thyroiditis, Autoimmune | ICF Syndrome | Conn Syndrome | Asplenia | Hypersomnia | Mucolipidosis | Ligneous Conjunctivitis | Bursitis | Hyperthyroidism | Pouchitis | Norrie Disease | Primary Cutaneous Amyloidosis | Pre-eclampsia | Potocki-Shaffer Syndrome | Purpura | Batten Disease | Pituitary Stalk Interruption Syndrome | Arthritis | Retinal Telangiectasia | Inflammatory Myofibroblastic Tumor | Non-small Cell Lung Cancer | Trigonocephaly | Oculocutaneous Albinism Type 4 | Insulin Resistance | Non-bullous Congenital Ichthyosiform Erythroderma | Amebiasis | Donnai-Barrow Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Chordoma | Pain | Congenital Hemolytic Anemia | Pyoderma Gangrenosum | Ocular Surface Squamous Neoplasia | Adenomyosis | Spina Bifida | Spinocerebellar Ataxia Type 16 | Pulmonary Vein Stenosis | Frontometaphyseal Dysplasia | Pachyonychia Congenita | Synpolydactyly | Erythropoietic Protoporphyria | Cholesteryl Ester Storage Disease | Hereditary Pyropoikilocytosis | Periodic Limb Movement Disorder | Facioscapulohumeral Muscular Dystrophy Type 2 | 3-methylglutaconic Aciduria Type IV | Cysticercosis | Multicystic Renal Dysplasia | Addison Disease | Scapuloperoneal Spinal Muscular Atrophy | Glomerulonephritis, Membranoproliferative | Bronchiectasis | Sclerocornea | Congenital Heart Block | Vestibular Disease | Blastomycosis | High Molecular Weight Kininogen Deficiency | Combined Malonic And Methylmalonic Acidemia | Shwachman-Bodian-Diamond Syndrome | Motor Neuron Diseases | Cancer, Bladder | Neurofibromatosis-Noonan Syndrome | Skin Fragility-woolly Hair Syndrome | Oligodendroglioma | Otitis Media | Delayed Sleep Phase Syndrome | Osteitis | Epidermodysplasia Verruciformis | Globozoospermia | Infectious Diarrhea | Osteoglophonic Dysplasia | Impetigo | Congenital Primary Aphakia | Meleda Disease | Dysequilibrium Syndrome | Open-angle Glaucoma | Fatty Aldehyde Dehydrogenase Deficiency | Hyperparathyroidism | Cryptosporidiosis | Pemphigus | Reflex Epilepsy | Bicuspid Aortic Valve | Chediak-Higashi Syndrome | Retinal Coloboma | Niemann-Pick Disease, Type B | Epidermolysis Bullosa | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Keloid | Familial Hemiplegic Migraine | Absence Epilepsy | Joubert Syndrome | Carbonic Anhydrase VA Deficiency | Nephroblastoma | Fetal And Neonatal Alloimmune Thrombocytopenia | Vitamin B12 Deficiency | Galactosialidosis | Prurigo Nodularis | Hermansky-Pudlak Syndrome | Hypogammaglobulinemia | Pierre Robin Syndrome | Chondromyxoid Fibroma | Neurodermatitis | Tylosis With Esophageal Cancer | Mohr-Tranebjaerg Syndrome | Pityriasis Rubra Pilaris | Kearns-Sayre Syndrome | Amyotrophic Lateral Sclerosis, Juvenile | Poikiloderma With Neutropenia | Beta-Propeller Protein-associated Neurodegeneration | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Syndactyly | Osteoarthritis | Waardenburg Syndrome Type 4 | Benign Hereditary Chorea | Farber Disease | Neurofibrosarcoma | Ocular Hypertension | Orthostatic Intolerance | Pterygium | Richter's Syndrome | Mast Cell Leukemia | Traboulsi Syndrome | Cystitis | Prune Belly Syndrome | Congenital Dyserythropoietic Anemia | Glaucoma | Hemosiderosis | Glycogen Storage Disease Type 1 | Carcinoma, Merkel Cell | Retinitis Pigmentosa 3 | Liver Failure | Wolfram Syndrome | Lichen Planus | Glycogen Storage Disease Type 0 | Charcot-Marie-Tooth Disease Type 2E | Hepatic Veno-occlusive Disease | Hereditary Coproporphyria | Constipation | Disseminated Intravascular Coagulation | Ornithine Transcarbamylase Deficiency | Protein C Deficiency | Niemann-Pick Disease, Type A | Primary Biliary Cholangitis | Congenital Central Hypoventilation Syndrome | Nestor-Guillermo Progeria Syndrome | Abetalipoproteinemia | Zellweger Syndrome | Onchocerciasis | Hypocalcemia | Huntington's Disease-like 2 | Polycystic Ovary Syndrome | Asphyxia Neonatorum | Lentigo | Lymphoma, Follicular | Inflammatory Bowel Disease | Liver Diseases | Congenital Hereditary Endothelial Dystrophy Type I | Sengers Syndrome | Angiosarcoma | Diabetes Insipidus | Multiple Hamartoma Syndrome | Placenta Previa | Optic Neuropathy | Cardiofaciocutaneous Syndrome | Haim-Munk Syndrome | Fetal Alcohol Syndrome | Cervicitis | Charcot-Marie-Tooth Disease Axonal Type 2N | Leiomyosarcoma | Warsaw Breakage Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Dyggve-Melchior-Clausen Disease | NGLY1 Deficiency | Pleurisy | Tuberculous Meningitis | Geleophysic Dysplasia | Low Phospholipid Associated Cholelithiasis | Holoprosencephaly | Phenylketonuria | Barakat Syndrome | Pulmonary Stenosis | Thrombophlebitis | Neurocysticercosis | Muscular Dystrophy | Retinal Diseases | Mucormycosis | Thanatophoric Dysplasia | Central Pain Syndrome | Dystonia-parkinsonism, X-linked | Spinocerebellar Ataxia Type 7 | Hypohidrotic Ectodermal Dysplasia, X-linked | Multiple Sclerosis, Primary Progressive | Waardenburg Syndrome | Chronic Lymphocytic Leukemia | Malignant Peripheral Nerve Sheath Tumor | Sjogren Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | D-2-Hydroxyglutaric Aciduria | Congenital Diaphragmatic Hernia | Leishmaniasis, Visceral | Trimethylaminuria | Relapsing Polychondritis | Spondylo-ocular Syndrome | Ataxia-ocular Apraxia 2 | Gynecomastia | Tetanus | Metatropic Dysplasia | Familial Exudative Vitreoretinopathy | Prolymphocytic Leukemia | Large Granular Lymphocytic Leukemia | Infantile Refsum Disease | Cleidocranial Dysplasia | VACTERL/VATER Association | Pulmonary Sclerosing Hemangioma | Sarcoma, Ewing | Down Syndrome | DNA Ligase IV Deficiency | Xeroderma Pigmentosum | Spondylosis | Choroiditis | Neuropathy | Tularemia | Veno-occlusive Disease | Primary Hyperoxaluria | Ollier Disease | Lafora Disease | Twin-to-twin Transfusion Syndrome | Becker Muscular Dystrophy | Hyper IgE Syndrome | Kleine-Levin Syndrome | Dystonia | Splenomegaly | Congenital Disorders Of Glycosylation Type II | Pure Autonomic Failure | Hepatic Steatosis | Pneumonia, Bacterial | Thanatophoric Dysplasia Type 1 | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Meningioma, Benign | Hennekam Lymphangiectasia-lymphedema Syndrome | Combined Deficiency Of Factor V And Factor VIII | Multiple Sclerosis, Relapsing-remitting | Thrombophilia | Charcot-Marie-Tooth Disease Type 4B1 | Language Disorders | Cranioectodermal Dysplasia | Chronic Granulomatous Disease, X-linked | Congenital Mirror Movements | Lung Diseases | Patent Foramen Ovale | Diverticulitis | Chronic Inflammatory Demyelinating Polyneuropathy