congenital tricuspid malformation
human disease
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congenital tricuspid malformation
Summary
congenital tricuspid malformation is a developmental defect during embryogenesis[1].
Key Facts
- congenital tricuspid malformation's instance of is recorded as developmental defect during embryogenesis[2].
- congenital tricuspid malformation's instance of is recorded as class of disease[3].
- congenital tricuspid malformation's subclass of is recorded as atrioventricular valve anomaly[4].
- congenital tricuspid malformation's subclass of is recorded as tricuspid valve disease[5].
- congenital tricuspid malformation's Orphanet ID is recorded as 98721[6].
- congenital tricuspid malformation's exact match is recorded as http://purl.obolibrary.org/obo/HP_0001702[7].
- congenital tricuspid malformation's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98721[8].
- congenital tricuspid malformation's UMLS CUI is recorded as C4025753[9].
- congenital tricuspid malformation's UMLS CUI is recorded as C5681691[10].
- congenital tricuspid malformation's Human Phenotype Ontology ID is recorded as HP:0001702[11].
- congenital tricuspid malformation's ICD-10-CM is recorded as Q22.8[12].
- congenital tricuspid malformation's ICD-10-CM is recorded as Q22.5[13].
- congenital tricuspid malformation's ICD-10-CM is recorded as Q22.9[14].
- congenital tricuspid malformation's ICD-10-CM is recorded as Q22.4[15].
- congenital tricuspid malformation's Mondo ID is recorded as MONDO_0020289[16].
- congenital tricuspid malformation's ICD-11 ID is recorded as LA87.0[17].
- congenital tricuspid malformation's ICD-11 ID is recorded as 995525654[18].