Pemphigus Foliaceus

About the Disease
Pemphigus Foliaceus, also known as superficial pemphigus, is related to pemphigus erythematosus and bullous impetigo. An important gene associated with Pemphigus Foliaceus is DSG1 (Desmoglein 1), and among its related pathways/superpathways are ERK Signaling and Innate Immune System. The drugs Prednisone and glucocorticoids have been mentioned in the context of this disorder. Affiliated tissues include skin, b cells and t cells, and related phenotypes are autoimmunity and acantholysis

Common Targets
SCN10A | RSBN1 | HLA-B | HLA-DRB1 | RMI2 | LINC01119 | HLA-DQA1 | LINC01176 | FCN3 | HLA-A | MOG | LINC-PINT | LNCRNA-IUR | LAIR1 | LAIR2 | PTPN22 | IGFL2 | MASP1 | LY86-AS1 | HLA-C | HLA-DQB1 | LOC93429 | SLC38A4 | CASC15 | CARMN | LINGO2 | KIR3DL2

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Other Diseases

Lymphedema | Gastroschisis | Schizencephaly | Melnick-Needles Syndrome | Burn-McKeown Syndrome | Congenital Tufting Enteropathy | Adenoid Cystic Carcinoma | Mitochondrial DNA Depletion Syndrome | X-linked Acrogigantism | Dental Caries | Pyruvate Dehydrogenase Deficiency | Intermittent Explosive Disorder | Chromosome 16p11.2 Deletion Syndrome | Holoprosencephaly | Chordoma | Alveolar Capillary Dysplasia | Sertoli Cell-only Syndrome | Hypogonadism | Retinal Coloboma | Niemann-Pick Disease, Type B | T-cell Lymphoma, Subcutaneous Panniculitis-like | Hyperphenylalaninemia | Raine Syndrome | Arthropathy | Joubert Syndrome 2 | WAGR Syndrome | Hemophilia | Macular Corneal Dystrophy | Carcinoma, Signet Ring Cell | Unverricht-Lundborg Syndrome | Blastomycosis | Connective Tissue Disorders | Adenoma, Pituitary | Hepatitis | Woodhouse-Sakati Syndrome | Pelizaeus-Merzbacher Disease | Scapuloperoneal Myopathy, X-linked Dominant | Diverticulitis | Keratitis-ichthyosis-deafness Syndrome | Primary 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Type II | Goldenhar Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Parkinson Disease 6, Autosomal Recessive Early-onset | Diabetes Type 2 | Distal Spinal Muscular Atrophy | T-cell Chronic Lymphocytic Leukemia | Granuloma Annulare | Osteoarthritis | Uterine Leiomyoma | Skin Fragility-woolly Hair Syndrome | Androgenic Alopecia | Dermatitis | GATA2 Deficiency | Urethritis | Osteoporosis, Postmenopausal | Stickler Syndrome | MELAS Syndrome | Hypertension, Pulmonary | Nemaline Myopathy 8 | Central Retinal Artery Occlusion | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | VACTERL/VATER Association | Thrombocytopenia | Klinefelter Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Glycogen Storage Disease Type 6 | Congenital Nystagmus | Infertility | Sickle Cell Anemia | Phenylketonuria | Fucosidosis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Hypoplastic Left Heart Syndrome | Hypersensitivity | Amblyopia | Nephropathy | B-cell 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