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| Term | nephronophthisis 3 | ID (Ontology) | DOID:0111114 (Human Disease) |
| Definition | A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the NPHP3 gene on chromosome 3q22. | ||
| Also Known As | "NPH3" ; "NPHP3" | ||
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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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autosomal recessive disease__ kidney disease_______________| nephronophthisis |__nephronophthisis 3 |
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| Is a | nephronophthisis | ||
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External Crossreferences & Linkouts
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MESH:C565780 MIM:604387 |
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