VACTERL Association

About the Disease
Vacterl Association, also known as vater association, is related to vacterl association, x-linked, with or without hydrocephalus and vacterl association with hydrocephaly, x-linked. An important gene associated with Vacterl Association is FANCL (FA Complementation Group L), and among its related pathways/superpathways are Signaling by Hedgehog and Neural Stem Cells and Lineage-specific Markers. The drugs Nicotinamide and Niacin have been mentioned in the context of this disorder. Affiliated tissues include kidney, trachea and heart, and related phenotypes are growth/size/body region and endocrine/exocrine gland

Common Targets
PCSK5 | LPP | HOXD13 | CHD7 | FANCL | FANCF

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Hepatitis, Autoimmune | Non-epidermolytic Palmoplantar Keratoderma | Bernard-Soulier Syndrome | Long QT Syndrome Type 2 | Carpal Tunnel Syndrome | Papulopustular Rosacea | Schnyder Crystalline Corneal Dystrophy | Hypocalcemia | Iron Deficiency Anemia | Polymicrogyria | Albinism | Hyperprolactinemia | Hereditary Inclusion Body Myopathy | Anorchia | Pyruvate Kinase Deficiency | Dysequilibrium Syndrome | Hoyeraal-Hreidarsson Syndrome | Urticaria | Werner's Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Zimmermann-Laband Syndrome | Cramp Fasciculation Syndrome | Acne | Leber Hereditary Optic Neuropathy | Hydronephrosis | T-cell Chronic Lymphocytic Leukemia | Knobloch Syndrome | Neurofibromatosis | Charcot-Marie-Tooth Disease, Type 2A | Hypotonia-cystinuria Syndrome | Anti-NMDA Receptor Encephalitis | Filariasis | Sarcoma, Ewing | Leri-Weill Dyschondrosteosis | Robinow Syndrome | Language Disorders | Diabetic Neuropathy | Hidradenitis Suppurativa | Congenital Heart Defects | 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