autosomal recessive disease Pierson syndrome DOID:0060852 GARD:0003945 GARD:0009420 ICD10:N04.8 MESH:C537185 MONDO:0012184 NCIT:C128145 OMIM:609049 Orphanet:2670 Pierson syndrome Pierson syndrome is characterised by the association of congenital nephrotic syndrome and ocular anomalies with microcoria. SCTID:723449004 UMLS:C1836876 https://rarediseases.info.nih.gov/diseases/9420/pierson-syndrome microcoria - congenital nephrosis microcoria - congenital nephrotic syndrome microcoria-congenital nephrosis syndrome microcoria-congenital nephrotic syndrome LAMB2-related infantile-onset nephrotic syndrome