Congenital nephrotic syndrome, Finnish type
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A rare congenital nephrotic syndrome characterized by massive protein loss and marked edema manifesting in utero 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
- ICD-10:N04.8 (Attributed (The ICD10 code is attributed by Orphanet))
- MedDRA:10060740 (E (Exact mapping: the two concepts are equivalent))
- UMLS:C0403399 (E (Exact mapping: the two concepts are equivalent))
- OMIM:256300 (E (Exact mapping: the two concepts are equivalent))
- MeSH:C535761 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:N04.8 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
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
- has_inheritance some autosomal recessive
- part_of some Genetic nephrotic syndrome
- has_age_of_onset some antenatal
- has_age_of_onset some infancy
- has_age_of_onset some neonatal