17q11 deletion (Q105756)
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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
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