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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
46,XX Gonadal Dysgenesis Epibulbar Dermoid 
46,Xx Gonadal Dysgenesis, Partial Or Complete, Autosomal 
46,XX sex reversal 1  
46,XX sex reversal 2  
46,XX sex reversal 3 
Hypergonadotropic Gonadal Dysgenesis XX Type, Short Stature, and Recurrent Metabolic Acidosis 
ovarian dysgenesis 1  
Ovarian Dysgenesis 10  
ovarian dysgenesis 2 +   
ovarian dysgenesis 3  
ovarian dysgenesis 4  
ovarian dysgenesis 5  
ovarian dysgenesis 6  
ovarian dysgenesis 7  
ovarian dysgenesis 8  
Ovarian Dysgenesis 9  
Characterized by severe nonsyndromic primary ovarian insufficiency with primary amenorrhea, hypoplastic or absent ovaries, and delayed bone age. Caused by homozygous mutation in the SPIDR gene on chromosome 8q11.
Perrault Syndrome 1  

Synonyms
Exact Synonyms: ODG9
Primary IDs: OMIM:619665
Definition Sources: OMIM:619665

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