Congenital nephrotic syndrome, Finnish type
http://www.orpha.net/ORDO/Orphanet_839
Congenital nephrotic syndrome, Finnish type is characterised by protein loss beginning during foetal life.
Synonyms: Finnish congenital nephrosis
Term info
database cross reference
- OMIM:256300 (E (exact mapping (the terms and the concepts are equivalent)))
- MeSH:C535761 (E (exact mapping (the terms and the concepts are equivalent)))
- ICD-10:N04.8 (NTBT (narrower term maps to a broader term))
- UMLS:C0403399 (E (exact mapping (the terms and the concepts are equivalent)))
- MedDRA:10060740 (E (exact mapping (the terms and the concepts are equivalent)))
- ICD-10:N04.8 (Attributed)
definition citation
orphanet
hasDbXref
OMIM:256300, MeSH:C535761, ICD-10:N04.8, MedDRA:10060740, UMLS:C0403399
notation
ORPHA:839
Term relations
Subclass of:
- disease
- present_in some Worldwide and has_point_prevalence_range some Unknown_epidemiological_range
- present_in some Finland and has_birth_prevalence_range some 1-5 / 10 000 and has_birth_prevalence_average_value value 12.2
- part_of some Congenital and infantile nephrotic syndrome
- has_inheritance some autosomal recessive
- has_age_of_onset some infancy
- has_age_of_onset some neonatal
Related from: