|
16Q24.3 Microdeletion Syndrome
Beckwith-Wiedemann syndrome +
branchiootorenal syndrome +
chromosomal deletion syndrome +
chromosomal duplication syndrome +
Chromosome 1, Deletion q21 q25
Chromosome 1, Monosomy 1p
Chromosome 1, Monosomy 1p22 p13
Chromosome 1, Monosomy 1p31 p22
Chromosome 1, Monosomy 1p32
Chromosome 1, Monosomy 1p34 p32
Chromosome 1, Monosomy 1q25 q32
Chromosome 1, Monosomy 1q32 q42
Chromosome 1, Monosomy 1q4
Chromosome 10, Monosomy 10q
Chromosome 11p, Partial Deletion
Chromosome 11q Partial Deletion
Chromosome 12p Partial Deletion
Chromosome 14q, Partial Deletions
Chromosome 14q, Terminal Deletion
Chromosome 15q, partial deletion
Chromosome 17, Deletion 17q23 q24
Chromosome 18, Deletion 18q23
Chromosome 2, Monosomy 2p22
Chromosome 2, Monosomy 2pter p24
Chromosome 2, Monosomy 2q
Chromosome 2, Monosomy 2q24
Chromosome 20, Deletion 20p
Chromosome 21, Monosomy 21q22
Chromosome 22, Microdeletion 22 q11
Chromosome 22, Monosome Mosaic
CHROMOSOME 2p16.3 DELETION SYNDROME
Chromosome 3, Monosomy 3p
Chromosome 3, Monosomy 3p14 p11
Chromosome 3, Monosomy 3p2
Chromosome 3, Monosomy 3p25
Chromosome 3, Monosomy 3q21 23
Chromosome 3, Monosomy 3q27
Chromosome 4 Short Arm Deletion
Chromosome 4, 4q Terminal Deletion Syndrome
Chromosome 4, Monosomy 4p14 p16
Chromosome 4, Monosomy 4q32
Chromosome 6 Ring Syndrome
Chromosome 6, Deletion 6q13 q15
Chromosome 6, Monosomy 6p23
Chromosome 6, Monosomy 6q
Chromosome 6, Monosomy 6q1
Chromosome 6, monosomy 6q2
Chromosome 7 Ring Syndrome
Chromosome 7, Monosomy 7q2
Chromosome 7, Monosomy 7q21
Chromosome 7, monosomy 7q3
Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB
Chromosome 8, Monosomy 8p
Chromosome 8, Monosomy 8p23 1
Chromosome 8, Monosomy 8q
Chromosome 8p Deletion Syndrome (partial)
Chromosome 9, Partial Monosomy 9p
Cornelia de Lange syndrome +
deafness, dystonia, and cerebral hypomyelination
Delayed Cranial Ossification due to CBFB Haploinsufficiency
Deletion 13q Syndrome, Partial
Distal Trisomy 10q Syndrome
Edinburgh Malformation Syndrome
Generalized Hypertrichosis Terminalis, with or without Gingival Hyperplasia
Intellectual Developmental Disorder, Autosomal Dominant, FRA12A Type
Isodicentric Chromosome 15 Syndrome
Male Sterility due to Y-Chromosome Deletions
mosaic variegated aneuploidy syndrome +
Pallister Killian Syndrome
Partial Duplication 15q Syndrome
Partial Trisomy 3q Syndrome
Prader-Willi-Like Syndrome Associated with Chromosome 6
Recombinant Chromosome 8 Syndrome
Ring Chromosome 4 Syndrome
ring chromosome syndrome +
Sex Chromosome Disorders +
Silver-Russell syndrome +
Warburton Anyane Yeboa Syndrome
X Chromosome, Monosomy Xp22 pter
X Chromosome, Monosomy Xq28
|
|