Diehtu doahpagis
Ávžžuhuvvon tearbma
Infant, Newborn, Diseases
Tiipa
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Topical Descriptor
Vuolledoahpagat
- 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
Stivrentearpmat
- Disease, Neonatal
- Diseases, Neonatal
- Neonatal Disease
- Neonatal Diseases
Muituimerkejupmi
- general only; for specific disease in newborn infant index specific disease + check tag INFANT, NEWBORN
Fuomášahttin
- 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.
Eará gielain
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Finnish
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neonataalisairaudet
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neonataalitaudit
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vastasyntyneen taudit
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Swedish
URI
http://www.yso.fi/onto/mesh/D007232
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