Nevus
Nevus
About the Disease
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi, also known as cloves syndrome, is related to hypomelanosis of ito and capillary hemangioma, and has symptoms including angina pectoris, back pain and chest pain. An important gene associated with Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi is PIK3CA (Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Alpha), and among its related pathways/superpathways are Innate Immune System and Signal Transduction. The drugs Miconazole and Clotrimazole have been mentioned in the context of this disorder. Affiliated tissues include skin, bone and kidney, and related phenotypes are hemihypertrophy and tethered cord
Common Targets
HRAS | LOC105370627 | TYR | GPNMB | PAX3 | GNAQ | VDR | PLA2G6 | DCT | G3845 | NCOA6 | NEK9 | LURAP1L-AS1 | CCDC140 | CDH11 | LOC105369749 | PPP1R3C | CLPTM1L | OCA2 | CDK10 | MIR196A2 | BAP1 | KIT | MAPK13 | TYRP1 | GNMT | KIR2DS1 | CLDN11 | GNA11 | MC1R | G673 | G7157 | GJB2 | NRAS | MYO7A
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Other Diseases
Chudley-McCullough Syndrome | Acute Lung Injury | Tendinopathy | Lymphomatoid Granulomatosis | Cryopyrin-associated Periodic Syndromes | Hypotrichosis | Mucolipidosis Type III | Pneumonia, Mycoplasma | Uremic Pruritus | Hypertension, Pulmonary | Porencephaly | Potocki-Shaffer Syndrome | Meier-Gorlin Syndrome | Hypotension, Orthostatic | Odonto-onycho-dermal Dysplasia | Mitochondrial DNA Depletion Syndrome 13 | Palmoplantar Keratoderma | Beckwith-Wiedemann Syndrome | Diabetes Mellitus, Transient Neonatal | Neurodegeneration With Brain Iron Accumulation | Chorioretinitis | Combined Pituitary Hormone Deficiency | Tietze Syndrome | 3C Syndrome | Papillon-Lefevre Syndrome | Dysequilibrium Syndrome | Gardner Syndrome | Acute Kidney Injury | Menkes Disease | Exotropia | Enlarged Vestibular Aqueduct | Atopy | Proteasome-associated Autoinflammatory Syndrome 2 | Acute Lymphocytic Leukemia | Phenylketonuria II | Wiskott-Aldrich Syndrome | Porphyria, Acute Intermittent | Sertoli Cell-only Syndrome 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Dehydrogenase X Deficiency | Acromegaly | Bladder Exstrophy | Syndactyly | Adult Polyglucosan Body Disease | Withdrawal Syndrome | Fundus Albipunctatus | Low Tension Glaucoma | Trichuriasis | Sarcomatoid Carcinoma Of The Lung | Neuronal Ceroid Lipofuscinosis | Open-angle Glaucoma | Lichen Sclerosus | Hypokalemic Periodic Paralysis | Intermittent Claudication | Adenylosuccinate Lyase Deficiency | Aarskog-Scott Syndrome | Stroke | Sporadic Inclusion Body Myositis | Gastroenteritis, Eosinophilic | Micro Syndrome | Hypertriglyceridemia | Nail-Patella Syndrome | Tetanus | Warsaw Breakage Syndrome | Chromosome 17q21.31 Deletion Syndrome | Infectious Diarrhea | Lentigo | Melnick-Needles Syndrome | Spitz Nevus | Cerebellar Ataxia, Cayman Type | Polymicrogyria | Avellino Corneal Dystrophy | Posterior Polar Cataract | Methylmalonic Acidemia | Hypolipoproteinemia | Hemoglobinopathies | Multiple System Atrophy | Multiple Myeloma | Apraxia | Ganglioglioma | Japanese Encephalitis | Pierpont Syndrome 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Desmosterolosis