Down syndrome
Description
A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.; OMIM mapping confirmed by DO. [SN].
Cell Lines
- NCHi010-A
- SDQLCHi065-A
- AHMUCNi004-A
- ICMi001-A
- ICMi001-B
- ICMi001-C
- ICMi002-A
- ICMi002-B
- ICMi002-C
- ICMi003-A
- ICMi003-B
- ICMi003-C
- ICMi004-A
- ICMi004-B
- ICMi004-C
- ICMi005-A
- ICMi005-B
- ICMi005-C
- ICMi006-A
- ICMi006-B
- ICMi006-C
- ICMi007-A
- ICMi007-B
- ICMi007-C
- ICMi008-A
- ICMi008-B
- ICMi008-C
- NCHi004-A
- NSi003-A
- NSi003-B
- UMICHe005-A
- SCVIi085-A
- SCVIi086-A
- UPSFRi005-A
- UPSFRi005-A-1
- UPSFRi005-A-1
- WISCi006-A