Chromosome 13Q14 Deletion Syndrome
Disease ID: disease_node_17115
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| Dbxref | ICD10CM:Q93.5, MIM:613884, ORDO:1587 |
|---|---|
| Subclassof | DOID_0050736, DOID_0060388 |
| Data Source | DOID |
| Synonyms | deletion 13q14 |
| Doid Label | chromosome 13q14 deletion syndrome |
| Doid Description | A chromosomal deletion syndrome that is characterized by low birth weight, dysmorphic facies, limb defects, genital malformations and psychomotor developmental delay, has_material_basis_in deletion of the long arm of chromosome 13. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17115 |
| Doid Id | DOID_0060391 |
| Label | Chromosome 13Q14 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)