Disease #05448 (NPHS-13 (nephrotic syndrome, type 13 (NPHS-13)), OMIM:616893)

Official abbreviation NPHS-13
Name nephrotic syndrome, type 13 (NPHS-13)
OMIM ID 616893
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NUP205
Associated tissues -
Disease features autosomal recessive?
Remarks -