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| Term | focal segmental glomerulosclerosis 3 | ID (Ontology) | DOID:0112245 (Human Disease) |
| Definition | A focal segmental glomerulosclerosis that has_material_basis_in loss of function mutation in the CD2AP gene on chromosome 6p12.3. | ||
| Also Known As | "FSGS3" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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monogenic disease |__autosomal genetic disease___________ glomerulosclerosis | |__focal segmental glomerulosclerosis__| focal segmental glomerulosclerosis 3 2 rec. |
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| Is a |
autosomal genetic disease focal segmental glomerulosclerosis |
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External Crossreferences & Linkouts
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| MIM:607832 | |||