Search Ontology:
Human Disease
focal segmental glomerulosclerosis 7
- Term ID
- DOID:0111132
- Synonyms
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- FSGS7
- Definition
- A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of the PAX2 gene on chromosome 10q24.31. https://www.ncbi.nlm.nih.gov/pubmed/24676634
- References
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- ICD10CM:N04.1
- MIM:616002
- Ontology
- Human Disease ( DOID:0111132 )
- is a type of
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Genes Involved
Zebrafish Models