has material basis in germline mutation in CLCN5 proteinuria proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/low_molecular_weight_proteinuria_with_hypercalciuric_nephrocalcinosis https://www.malacards.org/card/proteinuria_low_molecular_weight_with_hypercalciuria_and_nephrocalcinosis MONDO:0010644 DOID:0111815 OMIM:308990 UMLS:C1839874 Editor note: ORDO inclides a btnt xref to this from Dent disease type 1, presumably due to the fact proteinuria is sometimes a feature of dent disease. We capture this separately in annotations proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis MESH:C545036 proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis, X-linked recessive MEDGEN:333426 GARD:0015301 inherited kidney disorder