Disease-gene associations mined from literature

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,  DOID:0060390,  distal 10q deletion disease,  distal 10q deletion disorder,  chromosome 10q26 deletion syndrome ...