Chromosome 16P12.2-P11.2 Deletion Syndrome
Disease ID: disease_node_17109
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| Dbxref | ICD10CM:Q93.5, MIM:613604, ORDO:261211 |
|---|---|
| Subclassof | DOID_0060388 |
| Data Source | DOID |
| Synonyms | 16p11.2-p12.2 microdeletion syndrome, 16p11.2p12.2 microdeletion syndrome |
| Doid Label | chromosome 16p12.2-p11.2 deletion syndrome |
| Doid Description | A chromosomal deletion syndrome that has_material_basis_in a chromosome 16p12.2-p11.2 deletion and that is characterized by dysmorphic facial features, feeding difficulties, recurrent ear infections, developmental delay, and cognitive impairment. |
| Disease Node Id | disease_node_17109 |
| Doid Id | DOID_0060400 |
| Label | Chromosome 16P12.2-P11.2 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)