Infant, Newborn, Diseases

Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts.

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Subheadings:

Restrict to MeSH Major Topic.

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

Tree Number(s): C16.614

MeSH Unique ID: D007232

Entry Terms:

• Neonatal Diseases
• Disease, Neonatal
• Diseases, Neonatal
• Neonatal Disease

See Also:

• Congenital Abnormalities

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Infant, Newborn, Diseases
Amniotic Band Syndrome
Anemia, Neonatal
Fetofetal Transfusion
Fetomaternal Transfusion
Asphyxia Neonatorum
Birth Injuries
Neonatal Brachial Plexus Palsy
Paralysis, Obstetric
Colic
Congenital Bone Marrow Failure Syndromes
Congenital Hyperinsulinism
Nesidioblastosis
Cystic Fibrosis
Epilepsy, Benign Neonatal
Erythroblastosis, Fetal
Kernicterus
Hernia, Umbilical
Hydrophthalmos
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal +
Hyperostosis, Cortical, Congenital
Ichthyosis
Ichthyosiform Erythroderma, Congenital +
Ichthyosis Bullosa of Siemens
Ichthyosis, X-Linked
Sjogren-Larsson Syndrome
Infant, Premature, Diseases
Bronchopulmonary Dysplasia
Leukomalacia, Periventricular
Respiratory Distress Syndrome, Newborn +
Retinopathy of Prematurity
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
X-Linked Combined Immunodeficiency Diseases
Syphilis, Congenital
Thanatophoric Dysplasia
Thrombocytopenia, Neonatal Alloimmune
Toxoplasmosis, Congenital
Vitamin K Deficiency Bleeding
Wolman Disease