Inflammatory Linear Verrucous Epidermal Nevus

About the Disease
Inflammatory Linear Verrucous Epidermal Nevus, also known as verrucous epidermal nevus, is related to epidermolytic nevus and verrucous nevus acanthokeratolytic. Affiliated tissues include skin, pancreas and kidney.

Common Targets
PMVK | CARD14 | NSDHL

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Neovascular Glaucoma | Tularemia | Mesothelioma, Malignant | Transient Bullous Dermolysis Of The Newborn | Smith-Kingsmore Syndrome | Nephrotic Syndrome Type 1 | Renal Tubular Dysgenesis | Pyruvate Decarboxylase Deficiency | Charcot-Marie-Tooth Disease, Type 6 | Aspartylglycosaminuria | Urofacial Syndrome | Von Hippel-Lindau Disease | Acrodermatitis | Benign Hereditary Chorea | Thrombosis | Thalassemia, Beta | Silicosis | Progressive External Ophthalmoplegia | Saethre-Chotzen Syndrome | Intermittent Claudication | Chondrodysplasia Punctata | Congenital Hereditary Endothelial Dystrophy Type II | Osmotic Demyelination Syndrome | Antenatal Bartter Syndrome Type 1 | Acne | Plasma Cell Dyscrasia | Choroideremia | Carpenter Syndrome | Optic Nerve Hypoplasia, Bilateral | Pancreatitis | Glycogen Storage Disease Type 1 | Glycogen Storage Disease Type 0 | Optic Neuropathy | Anosmia, Congenital | Chronic Mucocutaneous Candidiasis | Infantile Liver Failure Syndrome 1 | Spinocerebellar Ataxia Type 16 | Hermansky-Pudlak Syndrome | Follicular Dendritic Cell Sarcoma | Postpartum Depression | Dystrophy, Cone-rod | Gingivitis | Opisthorchiasis | Congenital Heart Block | Hypothalamic Obesity | Cardiospondylocarpofacial Syndrome | Donnai-Barrow Syndrome | Vitamin A Deficiency | Kabuki Syndrome | Vitamin K Deficiency | Gerodermia Osteodysplastica | Blepharophimosis Syndrome | Feingold Syndrome | Lateral Meningocele Syndrome | Pneumonia, Viral | Aneurysm, Thoracic Aortic | 5-oxoprolinase Deficiency | Barrett Esophagus | Platelet Disorders | Hydrocephalus | Aneurysm, Abdominal Aortic | Smoldering Myeloma | Pityriasis Rubra Pilaris | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Imerslund-Grasbeck Syndrome | Intellectual Disability, Autosomal Dominant 5 | Androgen Insensitivity | Colon Adenoma | Sleep Disorder | Pure Red Cell Aplasia | Spasticity | Birt-Hogg-Dube Syndrome | Persistent Truncus Arteriosus | Acrocallosal Syndrome | Xeroderma Pigmentosum Variant Type | Sick Sinus 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Tuberculosis | Bainbridge-Ropers Syndrome | Apparent Mineralocorticoid Excess Syndrome | Spitz Nevus | Stuve-Wiedemann Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Kaposiform Hemangioendothelioma | Hypogonadism | Retinal Vasculitis | Paraganglioma, Carotid Body | Familial Retinal Arterial Macroaneurysm | Acute Anterior Uveitis | Neurotoxicity | Hyperparathyroidism, Primary | Gardner Syndrome | Craniofacial Dysostosis | Gastritis | Neuronal Ceroid Lipofuscinosis | Rhizomelic Chondrodysplasia Punctata | Pleurisy | Cyclic Vomiting Syndrome | Familial Dysautonomia | Acromesomelic Dysplasia | Keratoconjunctivitis | Cystinuria | Ocular Hypertension | Cutaneous Lupus Erythematosus | Acute Chest Syndrome | Autosomal Recessive Bestrophinopathy | Centronuclear Myopathy | Ocular Albinism Type 1 | Prolymphocytic Leukemia | Pyoderma Gangrenosum | Amelogenesis Imperfecta | Incontinentia Pigmenti | Spinocerebellar Ataxia Type 3 | Greig Cephalopolysyndactyly Syndrome | Liver Failure, Acute 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