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chromosome 13q14 deletion syndrome (DOID:0060391)
Alliance: disease page
Synonyms: deletion 13q14
Alt IDs: OMIM:613884, ICD10CM:Q93.5, ORDO:1587
Definition: 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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/17/2024
MGI 6.24 		The Jackson Laboratory