chromosome 14q11-q22 deletion syndrome
Also known as: 14q11.2 microdeletion syndrome, Del(14)(q11.2), chromosome 14q11-q22 deletion syndrome, chromosome 14q11-q22 deletion syndrome, isolated cases, monosomy 14q11.2
Additional Disease Briefs
chromosome 15q11.2 deletion syndrome
Also known as: 15q11.2 BP1-BP2 microdeletion syndrome, 15q11.2 microdeletion, 15q11.2 microdeletion syndrome, Del(15)(q11.2), chromosome 15q11.2 deletion, chromosome 15q11.2 deletion syndrome, chromosome 15q11.2 microdeletion, monosomy 15q11.2
chromosome 15q13.3 microdeletion syndrome
Also known as: 15q13.3 microdeletion, 15q13.3 microdeletion syndrome, Del(15)(q13.3), chromosome 15q13.3 deletion syndrome, chromosome 15q13.3 microdeletion syndrome, microdeletion 15q13.3 syndrome, monosomy 15q13.3
chromosome 15q24 deletion syndrome
Also known as: 15q24 microdeletion syndrome, 15q24 recurrent microdeletion syndrome, Del(15)(q24), WITKOS, Witteveen-Kolk syndrome, chromosome 15Q24 Duplication syndrome, chromosome 15q24 deletion syndrome, monosomy 15q24
chromosome 15q25 deletion syndrome
Also known as: chromosome 15q25 deletion syndrome
chromosome 15q26-qter deletion syndrome
Also known as: 15q26 deletion syndrome, Drayer syndrome, chromosome 15q26-qter deletion syndrome, chromosome 15q26-qter deletion syndrome, isolated cases, distal 15q deletion syndrome, distal monosomy 15q, distal monosomy type 15q, monosomy 15q26, telomeric 15q deletion syndrome
chromosome 16 inversion, 0.45-Mb
Also known as: chromosome 16 inversion, 0.45-Mb
chromosome 16 trisomy
Also known as: mosaic trisomy 16, trisomy 16, trisomy chromosome 16
chromosome 16p11.2 duplication syndrome
Also known as: 16p11.2 duplication, 16p11.2 duplication syndrome, 16p11.2 microduplication, AUTS14B, autism, susceptibility to, 14B, chromosome 16p11.2 duplication syndrome, proximal 16p11.2 microduplication syndrome, proximal dup(16)(p11.2), proximal trisomy 16p11.2, susceptibility to autism, 14B
chromosome 16p12.1 deletion syndrome, 520kb
Also known as: Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus), chromosome 16p12.1 deletion syndrome, chromosome 16p12.1 deletion syndrome, 520-KB, chromosome 16p12.1 deletion syndrome, type 520kb, fragile site 16P12, fragile site, Distamycin a type, Rare, fra(16)(p12.1)