Congenital nephrotic syndrome, Finnish type
Congenital nephrotic syndrome, Finnish type
Definition
Congenital nephrotic syndrome, Finnish type is characterized by protein loss beginning during fetal life.
Also known as congenital nephrotic syndrome - Finnish type, congenital nephrotic syndrome, Finnish type, Finnish congenital nephrosis, nephrotic syndrome - NPHS1 associated — per MONDO
Also identified as
- DOID 0080390 per MONDO
- NCIT C122795 per MONDO
- OMIM 256300 per MONDO
- Orphanet 839 per MONDO
- SCTID 197601003 per MONDO
- UMLS C0403399 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Adult mammalian kidney | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Adult mammalian kidney | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Genitourinary system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Genitourinary system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Renal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Renal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |