CLAPO syndrome

Summary

CLAPO syndrome is a developmental defect during embryogenesis^[1].

Key Facts

• CLAPO syndrome's instance of is recorded as developmental defect during embryogenesis^[2].
• CLAPO syndrome's instance of is recorded as class of disease^[3].
• CLAPO syndrome's subclass of is recorded as overgrowth syndrome^[4].
• CLAPO syndrome's subclass of is recorded as genetic vascular anomaly^[5].
• CLAPO syndrome's subclass of is recorded as complex vascular malformation with associated anomalies^[6].
• CLAPO syndrome's MeSH descriptor ID is recorded as C567763^[7].
• CLAPO syndrome's OMIM ID is recorded as 613089^[8].
• CLAPO syndrome's KEGG ID is recorded as H02297^[9].
• CLAPO syndrome's Orphanet ID is recorded as 168984^[10].
• CLAPO syndrome's genetic association is recorded as PIK3CA^[11].
• CLAPO syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_168984^[12].
• CLAPO syndrome's UMLS CUI is recorded as C2751313^[13].
• CLAPO syndrome's ICD-10-CM is recorded as Q87.3^[14].
• CLAPO syndrome's Mondo ID is recorded as MONDO_0013125^[15].
• CLAPO syndrome's ICD-11 ID is recorded as 415642712^[16].
• CLAPO syndrome's UniProt disease ID is recorded as DI-05367^[17].