Showing entry for True Hermaphroditism (disorder)

General Disease Information
BXGD Id	BXGD005656
Disease Name	True Hermaphroditism (disorder)
Disease CUI Id	C0266361
MeSH Codes	C16   C13   C12   C19
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000119
Human Phenotype Ontology Term	Abnormality of the genitourinary system
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations