Disease #02975 (NPHS3 (nephrotic syndrome, type 3 (NPHS-3)), OMIM:610725)
Official abbreviation |
NPHS3 |
Name |
nephrotic syndrome, type 3 (NPHS-3) |
OMIM ID |
610725 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
PLCE1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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