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ONTOLOGY REPORT - ANNOTATIONS


Term:Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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Accession:DOID:9004324 term browser browse the term
Definition: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.
Synonyms:exact_synonym: Congenital Disorder;   Congenital Disorders;   Neonatal Diseases and Abnormalities
 primary_id: MESH:D009358;   RDO:0003053
 subset: RGD_JBrowse_slim
For additional species annotation, visit the Alliance of Genome Resources.


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  disease 15984
    Developmental Diseases 9281
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8095
        Congenital Abnormalities + 4465
        Fetal Diseases + 227
        Hemorrhagic Shock and Encephalopathy Syndrome 0
        Infant, Newborn, Diseases + 426
        Sandestig-Stefanova Syndrome 1
        genetic disease + 7613
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.