| Disease Browser
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Parent Node:
 Infant, Newborn, Diseases (D007232) |
..Starting node
.. Asphyxia Neonatorum (D001238)
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Child Nodes:
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| ........Thoracolaryngopelvic dysplasia (C536517) |
Sister Nodes: |
..Amniotic Band Syndrome (D000652)  3
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..Anemia, Neonatal (D000751) 2
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..Asphyxia Neonatorum (D001238) 1
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..Birth Injuries (D001720) 1
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..Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal (C563463)
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..Congenital Hyperinsulinism (D044903) 2
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..Cutis Laxa-Marfanoid Syndrome (C563639)
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..Cystic Fibrosis (D003550) 4
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..Developmental Delay, Epilepsy, and Neonatal Diabetes (C565253)
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..Diabetes Mellitus, Transient Neonatal, 1 (C563322)
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..Diabetes Mellitus, Transient Neonatal, 2 (C563672)
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..Epilepsy, Benign Neonatal (D020936) 13
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..Erythroblastosis, Fetal (D004899) 7
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..Hernia, Umbilical (D006554) 6
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..Hydrophthalmos (D006871)
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..Hyperbilirubinemia, Neonatal (D051556) 4
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..Hypercalcemia, Idiopathic, of Infancy (C562581)
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..Hyperglycinemia, Transient Neonatal (C562672)
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..Hyperostosis, Cortical, Congenital (D006958) 6
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..Hyperparathyroidism, Neonatal Severe Primary (C563375)
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..Hypoglycemia, Neonatal, Simulating Foetopathia Diabetica (C565484)
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..Ichthyosis (D007057) 66
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..Infant, Premature, Diseases (D007235) 14
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..Meconium Aspiration Syndrome (D008471)
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..Mobius Syndrome (D020331) 4
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..Neonatal Abstinence Syndrome (D009357)
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..Nystagmus, Congenital (D020417) 17
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..Ophthalmia Neonatorum (D009878)
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..Persistent Fetal Circulation Syndrome (D010547) 1
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..Rothmund-Thomson Syndrome (D011038) 5
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..Sclerema Neonatorum (D012593)
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..Severe Combined Immunodeficiency (D016511) 22
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..Syphilis, Congenital (D013590)
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..Thanatophoric Dysplasia (D013796) 8
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..Thrombocytopenia, Neonatal Alloimmune (D054098)
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..Toxoplasmosis, Congenital (D014125)
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..Vitamin K Deficiency Bleeding (D006475)
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..Wolman Disease (D015223) 2
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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