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46,XY partial gonadal dysgenesis
Disease Summary
Associated Targets (14)
Tbio
10
Tclin
2
Tchem
2
Mondo Description 46,XY partial gonadal dysgenesis (46,XY PGD) is a disorder of sex development (DSD) associated with anomalies in gonadal development that results in genital ambiguity of variable degree ranging from almost female phenotype to almost male phenotype in a patient carrying a male 46,XY karyotype.
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:251510
SCTID:725045004
UMLS:C4510744
MONDO:0016674
High level summary of knowledge for a disease, including descriptions and datasource references.