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| Term | ovarian dysgenesis 2 | ID (Ontology) | DOID:0080494 (Human Disease) |
| Definition | A 46 XX gonadal dysgenesis that has_material_basis_in mutation in the BMP15 gene on chromosome Xp11. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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monogenic disease |__X-linked monogenic disease__ gonadal dysgenesis | |__46 XX gonadal dysgenesis____| ovarian dysgenesis 2 |
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Relationships
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| Is a |
X-linked monogenic disease 46 XX gonadal dysgenesis |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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MESH:C564499 MIM:300510 |
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