Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Diseases existing at birth and often before birth, or that develop during the first month of life (INFANT, NEWBORN, DISEASES), regardless of causation. Of these diseases, those characterized by structural deformities are termed CONGENITAL ABNORMALITIES.

Year introduced: 2002

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Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16

MeSH Unique ID: D009358

Entry Terms:

• Congenital Disorders
• Congenital Disorder
• Disorder, Congenital
• Disorders, Congenital
• Neonatal Diseases and Abnormalities

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Drug-Induced
Abnormalities, Multiple +
Abnormalities, Radiation-Induced
Abnormalities, Severe Teratoid +
Aicardi Syndrome
Cardiovascular Abnormalities +
Chromosome Disorders +
Congenital Microtia
Digestive System Abnormalities +
Eye Abnormalities +
Hernias, Diaphragmatic, Congenital
Lymphatic Abnormalities +
Musculoskeletal Abnormalities +
Nervous System Malformations +
Respiratory System Abnormalities +
Situs Inversus +
Skin Abnormalities +
Stomatognathic System Abnormalities +
Thyroid Dysgenesis +
Urogenital Abnormalities +
Fetal Diseases
Chorioamnionitis
Echogenic Bowel
Erythroblastosis, Fetal +
Fetal Alcohol Spectrum Disorders
Fetal Growth Retardation
Fetal Hypoxia
Fetal Macrosomia
Meconium Aspiration Syndrome
Nuchal Cord
Pyelectasis
Genetic Diseases, Inborn
Adrenal Hyperplasia, Congenital
Alagille Syndrome
alpha 1-Antitrypsin Deficiency
Anemia, Hemolytic, Congenital +
Anemia, Hypoplastic, Congenital +
Ataxia Telangiectasia
Autoimmune Lymphoproliferative Syndrome
Blood Coagulation Disorders, Inherited +
Brugada Syndrome
CADASIL
Camurati-Engelmann Syndrome
Cardiomyopathy, Hypertrophic, Familial
CHARGE Syndrome
Cherubism
Chromosome Disorders +
Ciliopathies +
Costello Syndrome
Cystic Fibrosis
Donohue Syndrome
Dwarfism +
Eye Diseases, Hereditary +
Familial Multiple Lipomatosis
Frasier Syndrome
GATA2 Deficiency
Genetic Diseases, X-Linked +
Genetic Diseases, Y-Linked
Hajdu-Cheney Syndrome
Hemoglobinopathies +
Hereditary Autoinflammatory Diseases +
Heredodegenerative Disorders, Nervous System +
Hyper-IgM Immunodeficiency Syndrome
Hyperthyroxinemia, Familial Dysalbuminemic
Imprinting Disorders +
Kallmann Syndrome
Kartagener Syndrome
Laminopathies +
Lennox Gastaut Syndrome
Loeys-Dietz Syndrome
Marfan Syndrome
Metabolism, Inborn Errors +
Muscular Dystrophies +
Myasthenic Syndromes, Congenital
Nail-Patella Syndrome
Neoplastic Syndromes, Hereditary +
Oculocerebrorenal Syndrome
Orofaciodigital Syndromes
Osteoarthropathy, Primary Hypertrophic
Osteochondrodysplasias
Osteogenesis Imperfecta
Pain Insensitivity, Congenital
Pelger-Huet Anomaly
Primary Immunodeficiency Diseases +
Pycnodysostosis
Renal Tubular Transport, Inborn Errors +
Skin Diseases, Genetic +
Werner Syndrome
Yellow Nail Syndrome
Infant, Newborn, Diseases
Amniotic Band Syndrome
Anemia, Neonatal +
Asphyxia Neonatorum
Birth Injuries +
Colic
Congenital Bone Marrow Failure Syndromes
Congenital Hyperinsulinism +
Cystic Fibrosis
Epilepsy, Benign Neonatal
Erythroblastosis, Fetal +
Hernia, Umbilical
Hydrophthalmos
Hyperbilirubinemia, Neonatal +
Hyperostosis, Cortical, Congenital
Ichthyosis +
Infant, Premature, Diseases +
Meconium Aspiration Syndrome
Mobius Syndrome
Neonatal Abstinence Syndrome
Neonatal Sepsis
Nystagmus, Congenital
Ophthalmia Neonatorum
Persistent Fetal Circulation Syndrome
Rothmund-Thomson Syndrome
Sclerema Neonatorum
Severe Combined Immunodeficiency +
Syphilis, Congenital
Thanatophoric Dysplasia
Thrombocytopenia, Neonatal Alloimmune
Toxoplasmosis, Congenital
Vitamin K Deficiency Bleeding
Wolman Disease