Term Name: chromosome 19q13.11 deletion syndrome
Synonyms: 19q13.11 microdeletion syndrome, monosomy 19q13.11
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.
Ontology: Human Disease [DOID:0060408]   ( DOID:0060408 )

Relationships
is a type of: autosomal dominant disease chromosomal deletion syndrome