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DOID:0060411 - chromosome 1q21.1 deletion syndrome
Disease Ontology Definition:A chromosomal deletion syndrome that has_material_basis_in a contiguous deletion of the 1q21.1 region on chromosome 1 and is characterized by an increases the risk of delayed development, intellectual disability, physical abnormalities, and neurological and psychiatric problems.
Synonyms: 1q21.1 microdeletion syndrome, monosomy 1q21.1,
Xenbase Genes : gja5, gja8
MONDO:0012914 - chromosome 1q21.1 deletion syndrome |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
chromosomal deletion syndrome (is_a)