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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
17-beta hydroxysteroid dehydrogenase 3 deficiency +   
46,XY sex reversal +   
46,XY sex reversal 1  
46,Xy True Hermaphroditism, Sry-Related  
androgen insensitivity syndrome +   
chondrodysplasia-pseudohermaphroditism syndrome  
Denys-Drash syndrome  
Frasier syndrome  
Kallmann syndrome +   
Leydig cell hypoplasia +   
Lipoid Congenital Adrenal Hyperplasia  
Male Pseudohermaphroditism due to Defective LH Molecule 
Male Pseudohermaphroditism/Mental Retardation Syndrome, Verloes Type 
persistent Mullerian duct syndrome  
Pseudovaginal Perineoscrotal Hypospadias  
Testicular Anomalies with or without Congenital Heart Disease  
Urioste Martinez-Frias Syndrome 
WAGR syndrome +   

Synonyms
Primary IDs: MESH:C567575 ;   RDO:0015622

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