Chromosome 15Q11.2 Deletion Syndrome
Disease ID: disease_node_17113
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| Dbxref | MIM:615656, ORDO:261183, UMLS_CUI:C3180937 |
|---|---|
| Subclassof | DOID_0050736, DOID_0060388 |
| Data Source | DOID |
| Synonyms | 15q11.2 microdeletion syndrome |
| Doid Label | chromosome 15q11.2 deletion syndrome |
| Doid Description | A chromosomal deletion syndrome that is characterized by intellectual disability, dysmorphic facies, psychiatric illness and autism spectrum disorder, has_material_basis_in autosomal domit inheritance of partial deletion of the long arm of chromosome 15. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17113 |
| Doid Id | DOID_0060393 |
| Label | Chromosome 15Q11.2 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)