Congenital nephrotic syndrome, Finnish type
Go to external page http://www.orpha.net/ORDO/Orphanet_839
A rare congenital nephrotic syndrome characterized by massive protein loss and marked edema manifesting <i>in utero</i> or during the first 3 months of life.
Synonyms:
Finnish congenital nephrosis
This is just here as a test because I lose it
Term information
database
cross reference
- MeSH:C535761 (E (Exact mapping: the two concepts are equivalent))
- UMLS:C0403399 (E (Exact mapping: the two concepts are equivalent))
- MedDRA:10060740 (E (Exact mapping: the two concepts are equivalent))
- OMIM:256300 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:N04.8 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Attributed (The ICD code is attributed by Orphanet).)
definition citation
- Orphanet
expertlink
- https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=839
hasDbXref
- MedDRA:10060740
- OMIM:256300
- UMLS:C0403399
- MeSH:C535761
- ICD-10:N04.8
has age of onset
- http://www.orpha.net/ORDO/Orphanet_409944
- http://www.orpha.net/ORDO/Orphanet_409943
- http://www.orpha.net/ORDO/Orphanet_409945
has birth prevalence range
- http://www.orpha.net/ORDO/Orphanet_409975
has inheritance
- http://www.orpha.net/ORDO/Orphanet_409930
has point prevalence range
- http://www.orpha.net/ORDO/Orphanet_409981
notation
- ORPHA:839
part of
- http://www.orpha.net/ORDO/Orphanet_564127
present in
- http://www.orpha.net/ORDO/Orphanet_410065
- http://www.orpha.net/ORDO/Orphanet_409991
Term relations
Subclass of: