Pierson syndrome
Pierson syndrome is characterised by the association of congenital nephrotic syndrome and ocular anomalies with microcoria
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Pierson syndrome
Summary
Pierson syndrome is a rare disease[1].
Key Facts
- Pierson syndrome's instance of is recorded as rare disease[2].
- Pierson syndrome's instance of is recorded as class of disease[3].
- Pierson syndrome's subclass of is recorded as autosomal recessive disease[4].
- Pierson syndrome's subclass of is recorded as nephrotic syndrome[5].
- Pierson syndrome's subclass of is recorded as primary glomerular disease[6].
- Pierson syndrome's subclass of is recorded as syndrome[7].
- Pierson syndrome's MeSH descriptor ID is recorded as C537185[8].
- Pierson syndrome's OMIM ID is recorded as 609049[9].
- Pierson syndrome's KEGG ID is recorded as H00576[10].
- Pierson syndrome's Disease Ontology ID is recorded as DOID:0060852[11].
- Pierson syndrome's Orphanet ID is recorded as 2670[12].
- Pierson syndrome's NCI Thesaurus ID is recorded as C128145[13].
- Pierson syndrome's health specialty is recorded as urology[14].
- Pierson syndrome's genetic association is recorded as LAMB2[15].
- Pierson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060852[16].
- Pierson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060852[17].
- Pierson syndrome's UMLS CUI is recorded as C1836876[18].
- Pierson syndrome's ICD-10-CM is recorded as N04.8[19].
- Pierson syndrome's GARD rare disease ID is recorded as 9420[20].
- Pierson syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
- Pierson syndrome's Mondo ID is recorded as MONDO_0012184[22].
- Pierson syndrome's UniProt disease ID is recorded as DI-02165[23].