Epidermolysis Bullosa

About the Disease
Epidermolysis Bullosa, also known as acantholysis bullosa, is related to epidermolysis bullosa simplex 1b, generalized intermediate and epidermolysis bullosa, junctional 1b, severe. An important gene associated with Epidermolysis Bullosa is KRT5 (Keratin 5), and among its related pathways/superpathways are ERK Signaling and Integrin Pathway. The drugs Morphine and Cholecalciferol have been mentioned in the context of this disorder. Affiliated tissues include skin, bone marrow and bone, and related phenotypes are growth/size/body region and immune system

Common Targets
DST | AMP-activated protein kinase (AMPK) | CNR2 | PLEC | TRPM8 | CHRNE | LAMB2 | CNR1 | EXPH5 | ITGA3 | KRT5 | LAMB3 | TRPV2 | TRPV1 | GZMB | MMP7 | COL17A1 | LAMC2 | DSP | KRT14 | MMP2 | TRPA1 | TACR1 | AGTR1 | PKP1 | CASP1 | LAMA3 | NLRP3 Inflammasome | IL1B | FERMT1 | ITGB4 | CD151 | ANPEP | G114548 | Collagen (nonspecified subtype) | GPR55 | MMP1 | COL7A1 | ITGA6

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Other Diseases

Granuloma Annulare | Charcot-Marie-Tooth Disease Type 2D | Multiple Sclerosis, Primary Progressive | Transient Bullous Dermolysis Of The Newborn | Uveitis, Anterior | Hypertrophy | Epidermolytic Hyperkeratosis | Basal Ganglia Disease | 3C Syndrome | Osteogenesis Imperfecta Type VI | Cushing Syndrome | Osteogenesis Imperfecta Type III | Glutaric Aciduria Type 2 | Spinocerebellar Ataxia Type 16 | Infantile Nephropathic Cystinosis | Hypersensitivity | Becker Muscular Dystrophy | Acute Leukemia | Holt-Oram Syndrome | Congenital Tufting Enteropathy | Myasthenia Gravis | Periodontitis | Ocular Albinism Type 1 | Echinococcosis | Scleritis | Emery-Dreifuss Muscular Dystrophy | Sjogren Syndrome | Vitamin D Deficiency | Sleep Apnea, Central | Choriocarcinoma | Fascioliasis | Erythema Multiforme | Mucolipidosis | Endophthalmitis | Blue Rubber Bleb Nevus Syndrome | SAPHO Syndrome | Chronic Idiopathic Myelofibrosis | Coffin-Siris Syndrome | Spastic Paraplegia Type 7 | Evans Syndrome | Lentigo | Sarcoma, Endometrial Stromal | Epicondylitis | Diabetic Neuropathy | Chronic Myeloid Leukemia | Optic Neuropathy | Cancer, Brain | Benign Recurrent Intrahepatic Cholestasis 1 | Charcot-Marie-Tooth Disease Type 4D | Aldosteronism | Meningioma | Polycystic Kidney, Autosomal Recessive | Poikiloderma With Neutropenia | Hypokalemic Periodic Paralysis | Fucosidosis | McLeod Syndrome | Necrotizing Autoimmune Myopathy | Spermatocele | Multiple Sclerosis, Chronic Progressive | Fuchs Heterochromic Iridocyclitis | Congenital Hypofibrinogenemia | Keratosis, Seborrheic | Cri-du-chat Syndrome | Bicuspid Aortic Valve | Erythropoietic Protoporphyria | Cousin Syndrome | Hypophosphatasia | Hereditary Folate Malabsorption | Pulmonary Capillary Hemangiomatosis | Robinow Syndrome | Castleman Disease | Camurati-Engelmann Disease | Optic Neuritis | Conjunctivitis | Spondyloperipheral Dysplasia | Intellectual Disability, Autosomal Dominant 5 | Myoclonus-dystonia Syndrome | Glycogen Storage Disease | Parkinson's Disease | Nephrotic Syndrome Type 1 | Familial Hypertrophic Cardiomyopathy | Panuveitis | Pulmonary Tuberculosis | Autosomal Recessive Spastic Paraplegia Type 75 | Hepatitis, Chronic | Arrhythmogenic Right Ventricular Cardiomyopathy | Polycystic Kidney, Autosomal Dominant | Cyclic Vomiting Syndrome | Keratosis, Actinic | Hypertension, Pulmonary | Cutaneous T-cell Lymphoma | Subacute Sclerosing Panencephalitis | Postpartum Depression | Hereditary Hemorrhagic Telangiectasia | Chronic Granulomatous Disease, X-linked | Autosomal Recessive Congenital Ichthyosis | Macrophagic Myofasciitis | Yellow Fever | Dementia | Pancytopenia | Prediabetes | Anorectal Fistula | Osteonecrosis Of The Jaw | Amyotrophic Lateral Sclerosis | Gangliosidosis | Bartsocas-Papas Syndrome | Leishmaniasis, Visceral | Coenzyme Q10 Deficiency | Cancer, Prostate | Gestational Trophoblastic Disease | Hepatic Veno-occlusive Disease | Sponastrime Dysplasia | Primary Hyperoxaluria | Metatropic Dysplasia | 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Syndrome | Crigler-Najjar Syndrome | Johanson-Blizzard Syndrome | CREST Syndrome | Spinal Muscular Atrophy Type 3 | Megalencephaly | Ichthyosis | Angiodysplasia | Hepatitis D | Traboulsi Syndrome | Familial Hyperaldosteronism | Pemphigus | Spasticity | Arteriovenous Malformations | Temporal Lobe Epilepsy | Alopecia | Glaucoma, Congenital | Neovascular Glaucoma | Asthma, Exercise-induced | Waardenburg Syndrome Type 2 | Encephalitis | Nephritis, Interstitial | Spitzoid Melanoma | Spinocerebellar Ataxia Type 2 | Pernicious Anemia | Acquired Partial Lipodystrophy | Bone Marrow Necrosis | Oral Lichen Planus | Extramammary Paget's Disease | Osteomyelitis | Cerebral Cavernous Malformations | Early Infantile Epileptic Encephalopathy | Facioscapulohumeral Muscular Dystrophy Type 2 | Hamartoma | Pheochromocytoma | Pituitary Dwarfism | Asplenia | Hypodontia | Myelomeningocele | Megaloblastic Anemia | Neurofibromatosis Type 1 | Anorexia Nervosa | Sarcoma | Lyme Disease | Eccrine Porocarcinoma | 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