| Term Name: | chromosome 14q11-q22 deletion syndrome |
|---|---|
| Synonyms: | 14q11.2 microdeletion syndrome |
| Definition: | A chromosomal deletion syndrome that is characterized by microcephaly, dysmorphic facies, psychomotor delay and failure to thrive, has_material_basis_in isolated cases of partial deletion of the long arm of chromosome 14. |
| Ontology: | Human Disease [DOID:0060392] ( DOID:0060392 ) |