Showing entry for Pure Gonadal Dysgenesis, 46, XX



                               
General Disease Information
BXGD IdBXGD009819
Disease NamePure Gonadal Dysgenesis, 46, XX
Disease CUI IdC0685837
MeSH Codes C16   C13   C12   C19  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations