2q32q33 deletion (Q60201): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 07:42, 14 August 2026
2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2015922071 |
||
| English | 2q32q33 deletion |
2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features. |
Statements
CID11:ID_2015922071
0 references
dki-india-ID_2015922071
0 references
Concluído
0 references
13 August 2026
0 references
