Crouzon Syndrome With Acanthosis Nigricans

About the Disease
Crouzon Syndrome with Acanthosis Nigricans, also known as crouzon syndrome-acanthosis nigricans syndrome, is related to luteoma and carpenter syndrome 1. An important gene associated with Crouzon Syndrome with Acanthosis Nigricans is FGFR3 (Fibroblast Growth Factor Receptor 3), and among its related pathways/superpathways are Breast cancer pathway and MAPK signaling pathway. Affiliated tissues include eye, skin and bone, and related phenotypes are frontal bossing and high forehead

Common Targets
FGFR3

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

Other Diseases

Autoimmune Interstitial Lung, Joint, And Kidney Disease | Bietti Crystalline Dystrophy | Hepatitis, Autoimmune | Hypersomnia | Lewy Body Dementia | Carcinoma, Transitional Cell | Sarcoma, Alveolar Soft Part | Primary Erythromelalgia | Chondrodysplasia Punctata | Creatine Deficiency Syndrome | Glycogen Storage Disease Type 1b | Synpolydactyly | Carotid Artery Disease | Liebenberg Syndrome | Anti-NMDA Receptor Encephalitis | GM2-gangliosidosis AB Variant | Craniolenticulosutural Dysplasia | Hyperekplexia | Vertigo | Imerslund-Grasbeck Syndrome | Primary Torsion Dystonia | Benign Familial Neonatal Convulsions | Cataract | GAPO Syndrome | Bethlem Myopathy | Homocystinuria | Thrombosis | Cat Eye Syndrome | Hemangioma | Saethre-Chotzen Syndrome | Stroke | Cholestasis, Intrahepatic | Diabetic Neuropathy | Trichothiodystrophy | Vascular Cognitive Impairment | Cancer, Bladder | Spinocerebellar Ataxia Type 20 | Diffuse Mesangial Sclerosis | Ganglioglioma | Pregnancy, Ectopic | Non-Langerhans Cell Histiocytosis | Noonan Syndrome-like Disorder With Loose Anagen Hair | Neurofibroma | Sclerosing Cholangitis | Congenital Myopathy | Nephrotic Syndrome Type 1 | Hereditary Sensory Neuropathy Type 1 | Osteoporosis-pseudoglioma Syndrome | Amyloidosis | Myasthenia | Antenatal Bartter Syndrome Type 1 | Eating Disorder | Congenital Dyserythropoietic Anemia | Conjunctivitis, Allergic | WAGR Syndrome | Myelodysplasia | Meningioma | Branchiootorenal Syndrome | Hyperlipidemia | Dysplastic Nevus | Polymicrogyria | Glioblastoma | Tibial Muscular Dystrophy | Cutaneous T-cell Lymphoma | Pyruvate Decarboxylase Deficiency | Chronic Kidney Disease | Arthropathy | Coronary Artery Disease | Tetanus | Mitochondrial DNA Depletion Syndrome | T-cell Chronic Lymphocytic Leukemia | Hereditary Spastic Paraplegia | Mitochondrial Myopathy | Neurodevelopmental Disorders | Hereditary Hemorrhagic Telangiectasia | Spinal And Bulbar Muscular Atrophy | Dystonia Musculorum Deformans | Metaphyseal Chondrodysplasia, Schmid Type | Leiomyoma | Holt-Oram Syndrome | Rolandic Epilepsy | Common Cold | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Marinesco-Sjogren Syndrome | Dermatofibrosarcoma | Fibronectin Glomerulopathy | Angiosarcoma Of The Breast | Hypolipoproteinemia | Cardiomyopathy, Peripartum | Parkinson's Disease | Spinocerebellar Ataxia Type 6 | Progressive Familial Intrahepatic Cholestasis Type 3 | Lyme Disease | Feingold Syndrome | Alexander Disease | Lymphangiomatosis | Anemia | Infantile Spasm | Cerebellofaciodental Syndrome | Sjogren Syndrome | Hemosiderosis | Cavitary Optic Disc Anomalies | Cartilage Disorders | Basal Ganglia Disease, Biotin-responsive | Insulinoma | Fetal Alcohol Syndrome | Pigment Dispersion Syndrome | Succinic Semialdehyde Dehydrogenase Deficiency | Dermatomyositis | Lymphoma, AIDS-related | Chronic Inflammatory Demyelinating Polyneuropathy | Monilethrix | Paroxysmal Kinesigenic Dyskinesia | Pulmonary Sclerosing Hemangioma | Gliosarcoma | Costello Syndrome | Chondrosarcoma | Muckle-Wells Syndrome | Spinocerebellar Ataxia Type 28 | GLUT1 Deficiency Syndrome | Bacterial Meningitis | Pelvic Inflammatory Disease | Heimler Syndrome | Peeling Skin Syndrome, Acral Type | Inflammatory Myofibroblastic Tumor | Mucolipidosis Type II | Pachyonychia Congenita | Incontinentia Pigmenti | Hemorrhoids | Cerebrotendinous Xanthomatosis | Esophagitis, Eosinophilic | Achromatopsia | Blue Rubber Bleb Nevus Syndrome | Familial Retinal Arterial Macroaneurysm | Familial Hemiplegic Migraine | Heroin Dependence | Juvenile Myoclonic Epilepsy | Fibromuscular Dysplasia | Situs Inversus | Ocular Surface Squamous Neoplasia | Pseudohermaphroditism | Bartsocas-Papas Syndrome | Congenital Disorders Of Glycosylation Type II | Infantile Liver Failure Syndrome 1 | Mood Disorder | Leiomyosarcoma | Walker-Warburg Syndrome | Chondrodysplasia Punctata 2, X-linked Dominant | Keratitis | Glycogen Storage Disease Type 9 | Congenital Dysfibrinogenemia | Placenta Previa | Graft-versus-host Disease | Congenital Nystagmus | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Kabuki Syndrome 2 | Rash | Hepatic Adenomatosis | Congenital Torticollis | VACTERL Association | Colitis, Collagenous | Hyperthermia, Malignant | Myeloid Leukemia | Precocious Puberty | Takotsubo Cardiomyopathy | Persistent Fetal Circulation | Uveitis | Sertoli Cell-only Syndrome | Charcot-Marie-Tooth Disease Type 4B1 | Myositis | Danon Disease | Twin-to-twin Transfusion Syndrome | Priapism | Familial Isolated Hyperparathyroidism | Corneal Dystrophy And Perceptive Deafness | Perivascular Epithelioid Cell Tumor | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Glycogen Storage Disease Type 4 | Heart Block | Osteogenesis Imperfecta Type VI | Eiken Syndrome | Liver Failure | Vitiligo | Charcot-Marie-Tooth Disease, Type 2 | Glutaric Aciduria Type 2 | Infantile Refsum Disease | Herpes Genitalis | Cerebral Amyloid Angiopathy | Thanatophoric Dysplasia | Sponastrime Dysplasia | Cenani-Lenz Syndactyly Syndrome | Ectodermal Dysplasia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Nemaline Myopathy 8 | Cancer, Lung | Lattice Corneal Dystrophy Type 1 | Histiocytosis | Lymphoproliferative Disease, X-linked | Cryptorchidism | Optic Nerve Hypoplasia, Bilateral | Long QT Syndrome Type 2 | Sclerosteosis 2 | Cirrhosis | Renal Tubular Acidosis | Small Lymphocytic Lymphoma | Kidney Stones | Snyder-Robinson Syndrome | Pompe Disease | Erythromelalgia | Thanatophoric Dysplasia Type 1 | Cardiomyopathy, Dilated, 1L | Raynaud Phenomenon | Familial Cerebral Amyloid Angiopathy | Congenital Nephrotic Syndrome | Neovascular Glaucoma | Focal Segmental Glomerulosclerosis | Primary Pigmented Nodular Adrenocortical Disease | Viral Meningitis | Mucolipidosis Type III | Pitt-Hopkins Syndrome | Cryptococcal Meningitis | Iron Deficiency Anemia | Urethritis | Meconium Ileus | Tricho-hepato-enteric Syndrome | Photosensitivity | Waldenstrom Macroglobulinemia | Menkes Disease | Dyggve-Melchior-Clausen Disease | Bronchiectasis | Polymyositis | Dyslipidemia | Primary Aldosteronism | Thrombophlebitis | Progressive Myoclonic Epilepsy | Relapsing Polychondritis | Hemimegalencephaly | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Coronary Heart Disease | Reflex Epilepsy | Intermittent Claudication | Progressive Familial Intrahepatic Cholestasis | Cardiac Arrest | Nephronophthisis | Retinal Dystrophy, Early-onset Severe | Glanzmann Thrombasthenia | Gout | Hepatorenal Syndrome | Gastritis | Actinomycetoma | Sarcomatoid Carcinoma Of The Lung | Intestinal Hypomagnesemia 1 | Trichotillomania | Vascular Calcification | Hypertensive Nephropathy | Spinocerebellar Ataxia Type 17 | Thyroid Dysgenesis | Anterior Segment Dysgenesis | 3-methylglutaconic Aciduria | Molybdenum Cofactor Deficiency | Primary Progressive Aphasia | Glutaric Aciduria Type 1 | Proteasome-associated Autoinflammatory Syndrome 2 | Chronic Neutrophilic Leukemia | Hypertension, Renal | Granuloma Annulare | MELAS Syndrome | Congenital Diaphragmatic Hernia | Varices | Double Outlet Right Ventricle | Diarrhea | Lymphoma, B-cell | Liver Diseases | Hepatitis B, Chronic | Rubeosis Iridis | Behavioral Variant Of Frontotemporal Dementia | Treacher Collins Syndrome | Hypopituitarism | D-2-Hydroxyglutaric Aciduria | Split Hand-foot Malformation | Riboflavin Transporter Deficiency Neuronopathy | Farber Disease | Herpes Simplex Dermatitis | Analgesia | Pseudoexfoliation Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Cancer, Skin | Periventricular Leukomalacia | Hypocalcemia | Ocular Albinism Type 1 | Loeys-Dietz Syndrome Type 4 | Retinoschisis | Hemangioendothelioma | Agammaglobulinemia | Blue Nevus | Inborn Errors Of Metabolism | Pure Autonomic Failure | Nicotine Addiction | Immunoproliferative Disorders | Rhizomelic Chondrodysplasia Punctata | Autosomal Recessive Spastic Paraplegia Type 35 | Facioscapulohumeral Muscular Dystrophy Type 1 | Angina Pectoris | Nail-Patella Syndrome | Leukocyte Adhesion Deficiency | Retinoblastoma | Sengers Syndrome | Peripheral T-cell Lymphoma | Pituitary Dwarfism | Pendred Syndrome | Pineoblastoma | Cryptosporidiosis | Jacobsen Syndrome | Cervical Dystonia | Androgenic Alopecia | Papillon-Lefevre Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Neuronal Ceroid Lipofuscinosis | Vasculitis | Autoimmune Autonomic Ganglionopathy | Stickler Syndrome | Galactosemia | Metabolic Diseases | Crouzon Syndrome With Acanthosis Nigricans | Nanophthalmos | Congenital Stromal Corneal Dystrophy | Chromosome 17q21.31 Deletion Syndrome | Oligoasthenoteratozoospermia | Systemic Mastocytosis | Schizophrenia | Richter's Syndrome | Retinitis Pigmentosa | Acne Vulgaris | Cerebrovascular Disorders | Duane Retraction Syndrome | Camptocormia | Eosinophilic Asthma | Spinal Muscular Atrophy | Fraser Syndrome | Hydronephrosis | Pemphigoid | Erysipelas | Alopecia Areata | Primary Lateral Sclerosis | Renal Failure | Primary Familial Brain Calcification | Fibrosarcoma | Oculocutaneous Albinism | Mandibuloacral Dysplasia With Type A Lipodystrophy | Nasodigitoacoustic Syndrome | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Geleophysic Dysplasia | Myoclonus-dystonia Syndrome | Cardiofaciocutaneous Syndrome | Malaria | Coloboma | 3-methylglutaconic Aciduria Type I | Beta-Propeller Protein-associated Neurodegeneration | Hyperoxaluria | Temporal Lobe Epilepsy | Lentigo | Heart Septal Defects | Plasma Cell Dyscrasia | Sleep Apnea | Hyperthyroidism | Conn Syndrome | Rhabdomyosarcoma, Alveolar | Dentinogenesis Imperfecta | Ophthalmia, Sympathetic | Coffin-Siris Syndrome | Asthma, Nocturnal | Muscle Wasting | Pleural Tuberculosis | Lipid Metabolism Disorders | Amish Infantile Epilepsy Syndrome | Hypoalbuminemia | Acute Leukemia | Keratoacanthoma | Nemaline Myopathy 10 | Optic Neuropathy | Intestinal Tuberculosis | Neurofibroma, Plexiform | Anencephaly | Liddle Syndrome | Potocki-Shaffer Syndrome | Mucolipidosis Type IV | Apparent Mineralocorticoid Excess Syndrome | Gyrate Atrophy Of The Choroid And Retina | Chromosome 16p11.2 Deletion Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Pneumonia, Viral | Spinocerebellar Ataxia Type 10 | Retinal Telangiectasia | Craniopharyngioma | Thymoma, Malignant | Multisystemic Smooth Muscle Dysfunction Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | X-linked Myotubular Myopathy | Familial Hypobetalipoproteinemia | Astrocytoma