| Metadata | |
|---|---|
| ID | DOID:0061194 |
| Name | nephrotic syndrome type 24 |
| 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/ |
| Xrefs | |
| Synonyms |
NPHS24 [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |