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Human Disease

nephrotic syndrome type 8

Term ID
DOID:0080389
Synonyms
Definition
A familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25. (2)
References
Ontology
Human Disease   ( DOID:0080389 )
Relationships
is a type of
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Genes Involved
Zebrafish Models