chromosome 19q13.11 deletion syndrome

Summary

DOID:0060408 - chromosome 19q13.11 deletion syndrome

Disease Ontology Definition:A chromosomal deletion syndrome that has_material_basis_in a chromosome 19q13.11 deletion and that is characterized by characterized by poor overall growth, slender habitus, microcephaly, delayed development, intellectual disability with poor or absent speech, and feeding difficulties.

Synonyms: 19q13.11 microdeletion syndrome, monosomy 19q13.11,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013090 - chromosome 19q13.11 deletion syndrome

MONDO:0013090 - chromosome 19q13.11 deletion syndrome

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), chromosomal deletion syndrome (is_a)