Human genes for distal 10q deletion syndrome
Distal 10q deletion syndrome [DOID:0060390]
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.
Synonyms: distal 10q deletion syndrome, distal 10q deletion disease, distal 10q deletion disorder, DOID:0060390, chromosome 10q26 deletion syndrome ...