Term info
database cross reference
- SCTID:48796009 (MONDO:equivalentTo)
- UMLS:CN043611 (MONDO:equivalentTo)
- UMLS:C3501848 (NCIT:C35337)
- DOID:2590 (MONDO:equivalentTo)
- OMIMPS:256300 (MONDO:equivalentTo)
- NCIT:C35337 (MONDO:equivalentTo)
definition
An instance of nephrotic syndrome that is caused by an inherited modification of the individual's genome.
exactMatch
http://linkedlifedata.com/resource/umls/id/CN043611, http://identifiers.org/snomedct/48796009, http://linkedlifedata.com/resource/umls/id/C3501848, http://purl.obolibrary.org/obo/NCIT_C35337, http://purl.obolibrary.org/obo/DOID_2590, https://omim.org/phenotypicSeries/PS256300
has exact synonym
hereditary nephrotic syndrome, congenital nephrotic syndrome
id
MONDO:0002350