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chromosome 1q41-q42 deletion syndrome (DOID:0060412)
Alliance: disease page
Synonyms: 1q41-q42 microdeletion syndrome; 1q41q42 microdeletion syndrome
Alt IDs: OMIM:612530, ICD10CM:Q93.5, ORDO:250999
Definition: A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 1q41-q42 region.

Disease References using Mouse Models (1)

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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory