Aplasia Cutis Congenita

About the Disease
Aplasia Cutis Congenita, Nonsyndromic, also known as congenital defect of skull and scalp, is related to corpus callosum, agenesis of and aplasia cutis congenita. An important gene associated with Aplasia Cutis Congenita, Nonsyndromic is BMS1 (BMS1 Ribosome Biogenesis Factor). Affiliated tissues include skin, bone and brain, and related phenotypes are failure to thrive and hip dysplasia

Common Targets
FGF3 | DOCK6 | TP63 | ANGPTL8 | EDAR | G3845 | BMS1 | GJB6 | WNT10A | KCTD1 | DLL4 | KREMEN1 | RBPJ | EOGT

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Glycogen Storage Disease Type 6 | Necrotizing Autoimmune Myopathy | Autosomal Recessive Congenital Ichthyosis | Renal Hypouricemia | Angiodysplasia | Thrombophilia | Methemoglobinemia | Sarcoma, Alveolar Soft Part | Intracerebral Hemorrhage | Dermatofibrosarcoma | Rhabdomyosarcoma, Alveolar | Primary Erythromelalgia | Neurodegeneration With Brain Iron Accumulation | Hypercholesterolemia | Hypotrichosis Simplex | Familial Exudative Vitreoretinopathy | Blepharoconjunctivitis | Pneumonia, Bacterial | Combined Pituitary Hormone Deficiency | Cataplexy | Choroideremia | Fucosidosis | Transthyretin-related Amyloidosis | Primary Progressive Nonfluent Aphasia | Lipid Metabolism Disorders | Wolcott-Rallison Syndrome | Schaaf-Yang Syndrome | Retinal Dystrophy, Early-onset Severe | Tinea | Hemochromatosis | Purpura, Thrombotic Thrombocytopenic | Anterior Segment Dysgenesis | Charcot-Marie-Tooth Disease, Type 2 | Benign Familial Neonatal Convulsions | Influenza | Sick Sinus Syndrome 1 | Primary 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