2q32q33 deletion (Q60201): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_2015922071 | |||
| Property / CURIE: CID11:ID_2015922071 / rank | |||
Normal rank | |||
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
