Nephrotic syndrome, type 26 - CISMeF

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CISMeF

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Nephrotic syndrome, type 26OMIM Phenotype

Preferred Label : Nephrotic syndrome, type 26;

Symbol : NPHS26;

Type : Phenotype, molecular basis known;

Prefixed ID : #620049;

Details

Origin ID

620049;

UMLS CUI

C5774221;

Genes related to phenotype
- Laminin, alpha-5 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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17/06/2025

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