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ovarian dysgenesis 1
Summary
- Definition
- A 46 XX gonadal dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16.
- Super Class
- 46 XX gonadal dysgenesis autosomal recessive disease
External Links
- Disease Ontology
- DOID:0080493
- Mondo Disease Ontology
- OMIM
Related Genes
