(Q55788409)
English
monosomy 21
Monosomy 21 is a chromosomal anomaly characterized by the loss of variable portions of a segment of the long arm of chromosome 21 that leads to an increased risk of birth defects, developmental delay and intellectual deficit
- 21q deletion syndrome
- 21q- syndrome
- Partial 21q monosomy
- Monosomy type 21
Statements
1 reference
1 reference
1 reference
C36469
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference