Disease #04010 (NPHS9 (nephrotic syndrome, type 9 (NPHS-9)), OMIM:615573)
Official abbreviation |
NPHS9 |
Name |
nephrotic syndrome, type 9 (NPHS-9) |
OMIM ID |
615573 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
ADCK4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|