Showing entry for Rett Syndrome, Preserved Speech Variant



                               
General Disease Information
BXGD IdBXGD014368
Disease NameRett Syndrome, Preserved Speech Variant
Disease CUI IdC1839332
MeSH Codes C16   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:150  
Disease Ontology Class Namedisease of mental health
Disorder Network disorder-protein-compound-food associations