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Human Disease

nephrotic syndrome type 24

Term ID
DOID:0061194
Synonyms
  • NPHS24
Definition
A familial nephrotic syndrome characterized by onset of proteinuria and hypoalbuminemia in early childhood, although onset in the second decade has been reported. that has_material_basis_in homozygous or compound heterozygous mutation in the DAAM2 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/33232676/
References
Ontology
Human Disease   ( DOID:0061194 )
Relationships
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Genes Involved
Zebrafish Models