mosaic trisomy 22

Summary

mosaic trisomy 22 is a developmental defect during embryogenesis^[1].

Key Facts

• mosaic trisomy 22's instance of is recorded as developmental defect during embryogenesis^[2].
• mosaic trisomy 22's instance of is recorded as class of disease^[3].
• mosaic trisomy 22's subclass of is recorded as total autosomal trisomy^[4].
• mosaic trisomy 22's subclass of is recorded as trisomy 22^[5].
• mosaic trisomy 22's MeSH descriptor ID is recorded as C536796^[6].
• mosaic trisomy 22's Orphanet ID is recorded as 96068^[7].
• mosaic trisomy 22's different from is recorded as trisomy 22^[8].
• mosaic trisomy 22's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_96068^[9].
• mosaic trisomy 22's UMLS CUI is recorded as C2931326^[10].
• mosaic trisomy 22's UMLS CUI is recorded as C2931327^[11].
• mosaic trisomy 22's ICD-10-CM is recorded as Q92.1^[12].
• mosaic trisomy 22's GARD rare disease ID is recorded as 6085^[13].
• mosaic trisomy 22's Mondo ID is recorded as MONDO_0019869^[14].