17q11 deletion (Q105756): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 12:12, 17 August 2026
17q11 microdeletion syndrome is a rare severe form of neurofibromatosis type 1, characterised by mild facial dysmorphism, developmental delay, intellectual deficit, and large number of neurofibromas.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_919770752 |
||
| English | 17q11 deletion |
17q11 microdeletion syndrome is a rare severe form of neurofibromatosis type 1, characterised by mild facial dysmorphism, developmental delay, intellectual deficit, and large number of neurofibromas. |
Statements
CID11:ID_919770752
0 references
dki-india-ID_919770752
0 references
Concluído
0 references
