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Congenital Disorder

Genetic Diseases, Inborn

AMW:DIS:160056

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.

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Genetic Diseases, Inborn has parent Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Neoplastic Syndromes, Hereditary has parent Genetic Diseases, Inborn
Hajdu-Cheney Syndrome has parent Genetic Diseases, Inborn
Dwarfism has parent Genetic Diseases, Inborn
Orofaciodigital Syndromes has parent Genetic Diseases, Inborn
Marfan Syndrome has parent Genetic Diseases, Inborn
Osteochondrodysplasias has parent Genetic Diseases, Inborn
Camurati-Engelmann Syndrome has parent Genetic Diseases, Inborn
Cherubism has parent Genetic Diseases, Inborn
Osteogenesis Imperfecta has parent Genetic Diseases, Inborn
Pycnodysostosis has parent Genetic Diseases, Inborn
Osteoarthropathy, Primary Hypertrophic has parent Genetic Diseases, Inborn
Nail-Patella Syndrome has parent Genetic Diseases, Inborn
Muscular Dystrophies has parent Genetic Diseases, Inborn
Costello Syndrome has parent Genetic Diseases, Inborn
Donohue Syndrome has parent Genetic Diseases, Inborn
Loeys-Dietz Syndrome has parent Genetic Diseases, Inborn
Alagille Syndrome has parent Genetic Diseases, Inborn
alpha 1-Antitrypsin Deficiency has parent Genetic Diseases, Inborn
Cystic Fibrosis has parent Genetic Diseases, Inborn
Kartagener Syndrome has parent Genetic Diseases, Inborn
CHARGE Syndrome has parent Genetic Diseases, Inborn
Oculocerebrorenal Syndrome has parent Genetic Diseases, Inborn
Ataxia Telangiectasia has parent Genetic Diseases, Inborn
CADASIL has parent Genetic Diseases, Inborn
Lennox Gastaut Syndrome has parent Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System has parent Genetic Diseases, Inborn
Myasthenic Syndromes, Congenital has parent Genetic Diseases, Inborn
Pain Insensitivity, Congenital has parent Genetic Diseases, Inborn
Eye Diseases, Hereditary has parent Genetic Diseases, Inborn
Adrenal Hyperplasia, Congenital has parent Genetic Diseases, Inborn
Frasier Syndrome has parent Genetic Diseases, Inborn
Kallmann Syndrome has parent Genetic Diseases, Inborn
Renal Tubular Transport, Inborn Errors has parent Genetic Diseases, Inborn
Brugada Syndrome has parent Genetic Diseases, Inborn
Cardiomyopathy, Hypertrophic, Familial has parent Genetic Diseases, Inborn
Anemia, Hypoplastic, Congenital has parent Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital has parent Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited has parent Genetic Diseases, Inborn
Hyper-IgM Immunodeficiency Syndrome has parent Genetic Diseases, Inborn
GATA2 Deficiency has parent Genetic Diseases, Inborn
Hemoglobinopathies has parent Genetic Diseases, Inborn
Pelger-Huet Anomaly has parent Genetic Diseases, Inborn
Autoimmune Lymphoproliferative Syndrome has parent Genetic Diseases, Inborn
Ciliopathies has parent Genetic Diseases, Inborn
Chromosome Disorders has parent Genetic Diseases, Inborn
Familial Multiple Lipomatosis has parent Genetic Diseases, Inborn
Genetic Diseases, X-Linked has parent Genetic Diseases, Inborn
Genetic Diseases, Y-Linked has parent Genetic Diseases, Inborn
Hereditary Autoinflammatory Diseases has parent Genetic Diseases, Inborn
Hyperthyroxinemia, Familial Dysalbuminemic has parent Genetic Diseases, Inborn
Imprinting Disorders has parent Genetic Diseases, Inborn
Laminopathies has parent Genetic Diseases, Inborn
Metabolism, Inborn Errors has parent Genetic Diseases, Inborn
Primary Immunodeficiency Diseases has parent Genetic Diseases, Inborn
Skin Diseases, Genetic has parent Genetic Diseases, Inborn
Werner Syndrome has parent Genetic Diseases, Inborn
Yellow Nail Syndrome has parent Genetic Diseases, Inborn

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