GenTIGSA Gene Database on Rare Genetic Disorders
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Pierson Syndrome  
Disease Aliases (15)

Lamb2-related infantile-onset nephrotic syndrome

Microcoria-congenital nephrotic syndrome

Microcoria - congenital nephrosis

Microcoria - congenital nephrotic syndrome

Microcoria and congenital nephrosis syndrome

Microcoria and congenital nephrotic syndrome

Microcoria-congenital nephrosis syndrome

Nephrotic syndrome, type 5, with ocular abnormalities

Nephrotic syndrome, type 5, without ocular abnormalities

Nphs5

Nephrotic syndrome, congenital, with ocular abnormalities and congenital myasthenic syndrome

Pierson syndrome

Nephrotic syndrome, type 5, with or without ocular abnormalities

Nephrotic syndrome, type 5, with or without ocular abnormalities; nphs5

Associated Genes (1)
 

NCBI-RefSeq:  LAMB2   (Laminin subunit beta 2)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of Pierson syndrome OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations