distal 10q deletion syndrome

Term ID

DOID:0060390

Synonyms

• chromosome 10q26 deletion syndrome
• distal monosomy 10q
• monosomy 10qter
• telomeric deletion 10q
• terminal chromosome 10q26 deletion syndrome

Definition

A chromosomal deletion syndrome that is characterized by developmental delay, intellectual disability, behavioral problems and facial facies caused by a missing copy of the long arm of chromosome 10. https://rarediseases.info.nih.gov/diseases/3711/chromosome-10q-deletion

References

• ICD10CM:Q93.5
• MESH:C567182
• OMIM:609625
• ORDO:96148

Ontology

Human Disease   ( DOID:0060390 )