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DO Term : chromosome 19q13.11 deletion syndrome [DOID:0060408] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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:
MESH:C567810,
19q13.11 microdeletion syndrome,
monosomy 19q13.11,
OMIM:613026,
UMLS_CUI:C2751651,
613026,
GARD:10592,
ORDO:217346

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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