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Ontology Browser
Term:
Congenital, Hereditary, and Neonatal Diseases and Abnormalities (DOID:9004324)
Annotations: Rat: (11401) Mouse: (10802) Human: (13665) Chinchilla: (9742) Bonobo: (10401) Dog: (10450) Squirrel: (9910) Pig: (10278)
Parent Terms Term With Siblings Child Terms
Developmental Disease +     
bone development disease +   
congenital heart disease +   
congenital structural myopathy +   
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.
fetal akinesia deformation sequence syndrome +   
Language Development Disorders +   
Neurodevelopmental Disorders +   
RADIO-TARTAGLIA SYNDROME  
RAUCH-STEINDL SYNDROME  
VERTEBRAL HYPERSEGMENTATION AND OROFACIAL ANOMALIES  
VISS syndrome  
YOON-BELLEN NEURODEVELOPMENTAL SYNDROME  

Synonyms
Exact Synonyms: Congenital Disorder ;   Congenital Disorders ;   Neonatal Diseases and Abnormalities
Primary IDs: MESH:D009358 ;   RDO:0003053
subset: RGD_JBrowse_slim
Definition Sources: MESH:D009358

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