Chromosome 1Q21.1 Deletion Syndrome
Disease ID: disease_node_17105
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| Dbxref | GARD:10813, ICD10CM:Q93.5, MIM:612474, ORDO:250989 |
|---|---|
| Subclassof | DOID_0060388 |
| Data Source | DOID |
| Synonyms | 1q21.1 microdeletion syndrome, monosomy 1q21.1 |
| Doid Label | chromosome 1q21.1 deletion syndrome |
| Doid Description | A chromosomal deletion syndrome that has_material_basis_in a contiguous deletion of the 1q21.1 region on chromosome 1 and is characterized by an increases the risk of delayed development, intellectual disability, physical abnormalities, and neurological and psychiatric problems. |
| Disease Node Id | disease_node_17105 |
| Doid Id | DOID_0060411 |
| Label | Chromosome 1Q21.1 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)