Chromosome 1Q41-Q42 Deletion Syndrome
Disease ID: disease_node_17025
Connections displayed (default: 10).
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| Dbxref | GARD:3738, ICD10CM:Q93.5, MIM:612530, ORDO:250999 |
|---|---|
| Subclassof | DOID_0060388, DOID_4621, DOID_0050739 |
| Data Source | DOID |
| Synonyms | 1q41-q42 microdeletion syndrome, 1q41q42 microdeletion syndrome |
| Doid Label | chromosome 1q41-q42 deletion syndrome |
| Doid Description | A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 1q41-q42 region. |
| Has Material Basis In | GENO_0000934 |
| Disease Node Id | disease_node_17025 |
| Doid Id | DOID_0060412 |
| Label | Chromosome 1Q41-Q42 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Genetic Disease(ID:disease_node_15586) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Holoprosencephaly(ID:disease_node_8636) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)