Search Ontology:
Human Disease
nephrotic syndrome type 18
- Term ID
- DOID:0080393
- Synonyms
-
- Definition
- A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42. https://www.ncbi.nlm.nih.gov/pubmed/30179222
- References
- Ontology
- Human Disease ( DOID:0080393 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models