general/autosomal-monosomies-and-deletions

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2p15-16.1 microdeletion syndrome
general/autosomal-monosomies-and-deletions
22q13 deletion syndrome

Rare genetic syndrome

general/autosomal-monosomies-and-deletions
Jacobsen syndrome
general/autosomal-monosomies-and-deletions
Koolen–De Vries syndrome

Rare genetic disorder caused by a deletion of six genes

general/autosomal-monosomies-and-deletions
1p36 deletion syndrome
general/autosomal-monosomies-and-deletions
Cri du chat syndrome

Human medical condition

general/autosomal-monosomies-and-deletions
18p-

Deletion of the short arm of chromosome 18

general/autosomal-monosomies-and-deletions
Kleefstra syndrome
general/autosomal-monosomies-and-deletions
Wolf–Hirschhorn syndrome

Chromosomal deletion syndrome

general/autosomal-monosomies-and-deletions
Smith–Magenis syndrome

Human disease

general/autosomal-monosomies-and-deletions
Monosomy 14

Genetic disorder

general/autosomal-monosomies-and-deletions
Monosomy 9p
general/autosomal-monosomies-and-deletions
Proximal 18q-
general/autosomal-monosomies-and-deletions
Distal 18q-

Human disease

general/autosomal-monosomies-and-deletions
TAR syndrome
general/autosomal-monosomies-and-deletions
WAGR syndrome
general/autosomal-monosomies-and-deletions
3q29 microdeletion syndrome
general/autosomal-monosomies-and-deletions