Epithelioid Hemangioma

About the Disease
Histiocytoid Hemangioma, also known as angiolymphoid hyperplasia with eosinophilia, is related to skin epithelioid hemangioma and hemangioma. An important gene associated with Histiocytoid Hemangioma is MALAT1 (Metastasis Associated Lung Adenocarcinoma Transcript 1), and among its related pathways/superpathways are Regulation of nuclear SMAD2/3 signaling and AP-1 transcription factor network. Affiliated tissues include bone, skin and tongue, and related phenotypes are neoplasm and immune system

Common Targets
G3845 | MAP2K1

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

Other Diseases

Adenomatoid Tumor | Rhinitis | Pathological Gambling | L-2-Hydroxyglutaric Aciduria | Becker Muscular Dystrophy | Hernia, Inguinal | H Syndrome | Retinal Telangiectasia | Wieacker-Wolff Syndrome | Keratitis-ichthyosis-deafness Syndrome | Epidermolytic Hyperkeratosis | Benign Recurrent Intrahepatic Cholestasis 1 | Osteosclerosis | Hypothyroidism | Alopecia Totalis | NGLY1 Deficiency | Pierpont Syndrome | Compartment Syndrome | Insulin Resistance | Congenital Ichthyosiform Erythroderma | Clouston Hidrotic Ectodermal Dysplasia | Polycythemia | Vasculitis | Adenoma, Pituitary | Astrocytoma | Muscular Dystrophy | Anterior Segment Dysgenesis | Wolfram Syndrome | Van Der Knaap Disease | Osteonecrosis Of The Jaw | Ganglioneuroma | Facioscapulohumeral Muscular Dystrophy Type 1 | Ovarian Sex Cord-stromal Tumor | Christianson Syndrome | Peritonitis | Graft-versus-host Disease | Tetanus | Usher Syndrome Type II | Mood Disorder | Benign Hereditary Chorea | Hyperthyroidism | Renpenning Syndrome | Peroxisomal Disorder | Silver-Russell Syndrome | Papillorenal Syndrome | Torticollis | Werner's Syndrome | Spondylolisthesis | Mitochondrial Myopathy | Hartsfield Syndrome | Metabolic Syndrome | Fucosidosis | Charcot-Marie-Tooth Disease | Hyperkeratosis | Meleda Disease | Granular Corneal Dystrophy | Congenital Stationary Night Blindness | Congenital Sodium Diarrhea | Lysosomal Acid Lipase Deficiency | Peeling Skin Syndrome, Acral Type | Takayasu's Arteritis | Carney-Stratakis Syndrome | Down Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Usher Syndrome Type I | Hemochromatosis Type 2 | Neuronal Ceroid Lipofuscinosis | Dysferlinopathy | Waardenburg Syndrome Type 2A | Hepatorenal Syndrome | Microcephaly | Asphyxia Neonatorum | Neurofibromatosis Type 2 | Temtamy Preaxial Brachydactyly Syndrome | Cardiac Arrest | Pterygium | Hyperferritinemia-cataract Syndrome | Vitelliform Macular Dystrophy | Lymphangioleiomyomatosis | Agammaglobulinemia | Sturge-Weber Syndrome | Fowler's Syndrome | Takotsubo Cardiomyopathy | Triphalangeal Thumb-polysyndactyly Syndrome | Kashin-Beck Disease | Thin Basement Membrane Disease | Congenital Hypofibrinogenemia | Gastric Atrophy | Pneumonia, Viral | Autosomal Recessive Congenital Ichthyosis | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Hoyeraal-Hreidarsson Syndrome | Leukodystrophies | Premature Ejaculation | HUPRA Syndrome | T-cell Leukemia | Polydactyly | Chronic Myelomonocytic Leukemia | Familial Hyperaldosteronism | Nance-Horan Syndrome | Sialidosis | Renal Medullary Carcinoma | Fontaine Progeroid Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Sensorineural Hearing Loss | COACH Syndrome | Spondylosis | Double Outlet Right Ventricle | Malaria | Currarino Syndrome | CREST Syndrome | Trichotillomania | Hereditary Pyropoikilocytosis | Antley-Bixler Syndrome | Costello Syndrome | Ghosal Syndrome | Pain | Osteoglophonic Dysplasia | Joubert Syndrome | Pulmonary Alveolar Proteinosis | Infertility, Male | Cancer, Kidney | Osteoporosis | Delirium | Crisponi Syndrome | Hepatitis, Alcoholic | Budd-Chiari Syndrome | Megaloblastic Anemia | Primary Hyperoxaluria | T-cell Chronic Lymphocytic Leukemia | Retinopathy Of Prematurity | Bietti Crystalline Dystrophy | Tonsillitis | Endometrial Hyperplasia | Arthropathy | Batten Disease | Hyperbilirubinemia | Kohlschutter-Tonz Syndrome | DEND Syndrome | Syncope | Carbamoyl Phosphate Synthetase I Deficiency | Melanoma | Chorea | ADNP Syndrome | Klippel-Feil Syndrome | Lentigo | Danon Disease | Agnathia-Otocephaly Complex | Intestinal Obstruction | Retinal Coloboma | Idiopathic Multicentric Castleman Disease | Hyperhomocysteinemia | Lipid Storage Myopathy | Benign Familial Pemphigus | HIBCH Deficiency | Neurofibroma, Plexiform | Charcot-Marie-Tooth Disease, Type 6 | Acute Generalized Exanthematous Pustulosis | Multiple Sclerosis | Adrenal Insufficiency | Glycogen Storage Disease Type 5 | Lattice Corneal Dystrophy Type 1 | Schwannoma | Cerebellofaciodental Syndrome | Mannosidase Deficiency Diseases | Gingivitis | Cholesteryl Ester Storage Disease | Amyotrophic Lateral Sclerosis, Juvenile | Ureteropelvic Junction Obstruction | Williams Syndrome | Ocular Albinism Type 1 | Hemochromatosis | Cerebral Amyloid Angiopathy | Gastroenteritis, Eosinophilic | Meningioma | Hemophilia | Deafness, Dystonia, And Cerebral Hypomyelination | Dystonia-parkinsonism, X-linked | Uremia | Hereditary Sensory Neuropathy Type 1 | Congenital Disorders Of Glycosylation | Seborrheic Dermatitis | Hemangioendothelioma | Choroiditis | Low Phospholipid Associated Cholelithiasis | Pseudo-pseudohypoparathyroidism | Intestinal Pseudo-obstruction | Spinal Cord Diseases | Spondyloepiphyseal Dysplasia Tarda, X-linked | Palmoplantar Keratoderma | Borjeson-Forssman-Lehmann Syndrome | Sleep Apnea, Obstructive | Sezary Syndrome | Lateral Meningocele Syndrome | Thyroid Hormone Resistance | Frontometaphyseal Dysplasia | Cramp Fasciculation Syndrome | Congenital Afibrinogenemia | C3 Glomerulopathy | Hypertension, Pulmonary | Kleine-Levin Syndrome | Sulfite Oxidase Deficiency | Xeroderma Pigmentosum Variant Type | Scoliosis | Hereditary Elliptocytosis | Neurocutaneous Melanocytosis | Juvenile Hyaline Fibromatosis | Saethre-Chotzen Syndrome | Craniolenticulosutural Dysplasia | Desbuquois Syndrome | Chondrodysplasia Punctata | Central Pain Syndrome | Esophageal Adenocarcinoma | Stargardt Disease | Glycogen Storage Disease Type 1 | Hepatitis A | Pregnancy, Ectopic | B-cell Prolymphocytic Leukemia | Nevus | DNA Ligase IV Deficiency | Hepatitis | Pycnodysostosis | Spinocerebellar Ataxia Type 13 | Aldosterone Deficiency | Erythema Multiforme | Fibrosarcoma | Influenza | Hepatic Adenomatosis | Macrodactyly | Hereditary Sensory And Autonomic Neuropathy | Tracheal Disorders | Zollinger-Ellison Syndrome | Proximal Symphalangism | Sitosterolemia | Metaphyseal Chondrodysplasia, Schmid Type | Kabuki Syndrome 2 | Azoospermia | Acute Coronary Syndrome | Desmosterolosis | Purpura, Thrombotic Thrombocytopenic | Dysthymia | Rolandic Epilepsy | Disseminated Intravascular Coagulation | Hypotrichosis | Obsessive-compulsive Disorder | Molybdenum Cofactor Deficiency | Common Cold | Infantile Nephropathic Cystinosis | Chitayat Syndrome | Early Infantile Epileptic Encephalopathy 4 | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Periventricular Leukomalacia | Hyperinsulinism-hyperammonemia Syndrome | Thymoma, Malignant | LRBA Deficiency | Hodgkin Lymphoma | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Hidradenitis Suppurativa | Restless Legs Syndrome | Vestibular Disease | Stuttering | Sarcoma, Ewing | Mandibuloacral Dysplasia With Type A Lipodystrophy | Pearson Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Postpoliomyelitis Syndrome | Fibrosis | Leiomyoma | Irritable Bowel Syndrome | Thyroid Dyshormonogenesis | Hydrocephalus, Normal Pressure | Multicystic Renal Dysplasia | Growth Hormone Excess | Methylmalonic Aciduria And Homocystinuria, CblC Type | Gastroschisis | Asplenia | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Immunoproliferative Disorders | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Cerebrovascular Disorders | Seminoma | Antisynthetase Syndrome | Intellectual Disability, Autosomal Dominant 5 | Neuroectodermal Tumors, Primitive | Senior-Loken Syndrome | Epidermolysis Bullosa Acquisita | Aphasia | Pelizaeus-Merzbacher Disease | Corneal Dystrophies, Hereditary | Rheumatic Heart Disease | Rheumatoid Arthritis | Familial Retinal Arterial Macroaneurysm | Chronic Periodontitis | Sandhoff Disease | Hereditary Hemorrhagic Telangiectasia Type 2 | Enterocolitis, Necrotizing | Renal Tubular Acidosis | Chiari Malformation Type I | Trismus-pseudocamptodactyly Syndrome | Avian Influenza | Blepharospasm | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Migraine | Osteopathia Striata With Cranial Sclerosis | Periodontitis | Wolfram Syndrome 2 | Muir-Torre Syndrome | Hypophosphatasia | Sjogren Syndrome | Corneal Dystrophy | Loeys-Dietz Syndrome Type 4 | Hereditary Spastic Paraplegia | Inborn Errors Of Metabolism | Partington Syndrome | Iron Deficiency Anemia | Depression | Fibronectin Glomerulopathy | Hypopigmentation | Epilepsy, Generalized | Diffuse Mesangial Sclerosis | Pemphigoid | Niemann-Pick Disease, Type B | Gangliosidosis, GM1 | Kindler Syndrome | Primary Erythromelalgia | Myoclonic Atonic Epilepsy | Cancer, Bladder | Carbohydrate Metabolism Disorders | Low Tension Glaucoma | Glaucoma | Diffuse Palmoplantar Keratoderma | Conduct Disorder | Ectopia Lentis, Isolated, Autosomal Recessive | Hyperoxaluria | Thrombosis | Infectious Diarrhea | Charcot-Marie-Tooth Disease Type 3 | Bronchiectasis | Cryoglobulinemia | Plasma Cell Dyscrasia | Insulinoma | Retinitis | Heterotopic Ossification | Lassa Fever | Bursitis | Non-Langerhans Cell Histiocytosis | Cyst | Fibromuscular Dysplasia | Dyslipidemia | Mucolipidosis | Congenital Dyserythropoietic Anemia Type 1 | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Intracranial Hypertension | Spitzoid Melanoma | Diabetes Type 1 | Keratocystic Odontogenic Tumor | Vitamin B12 Deficiency | Geleophysic Dysplasia | Hypocalcemia | Optic Nerve Hypoplasia, Bilateral | Varices | Melanocytic Nevus | Bullous Pemphigoid | Best Macular Dystrophy | Postaxial Polydactyly | Diabetes Mellitus, Transient Neonatal | Prurigo Nodularis | Follicular Dendritic Cell Sarcoma | Hypertension, Portal | Alpha-mannosidosis | Keratitis | Pyruvate Carboxylase Deficiency Disease | Vitamin D Deficiency | ACTH-independent Macronodular Adrenal Hyperplasia | Limb Girdle Muscular Dystrophy | Temporal Lobe Epilepsy | Agoraphobia | Holoprosencephaly | Speech Disorders | DRESS Syndrome | Neuroleptic Malignant Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Early Infantile Epileptic Encephalopathy | Cavitary Optic Disc Anomalies | Richter's Syndrome | Hyperinsulinemic Hypoglycemia | Scapuloperoneal Spinal Muscular Atrophy | Pulmonary Sclerosing Hemangioma | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Anti-glomerular Basement Membrane Disease | Dystonia | Rickets | Congenital Disorders Of Glycosylation Type II | Fragile X Syndrome | Primary Carnitine Deficiency | Stiff-man Syndrome | Miyoshi Myopathy | Dementia, Vascular | Martsolf Syndrome | Multiple System Atrophy