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Syndrome caused by partial chromosomal deletion

MONDO:0000761

A chromosomal disorder consisting of the absence of a part of a chromosome.

Also known as: microdeletion syndrome, chromosomal deletion syndrome

51 clinical trials for this condition and its sub-types.

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Sub-types

Williams syndrome (17) DiGeorge syndrome (8) 22q11.2 deletion syndrome (5) Chromosome 17p deletion (5) Smith-Magenis syndrome (4) Spermatogenic failure, Y-linked, 2 (4) Hereditary neuropathy with liability to pressure palsies (3) Myelodysplastic syndrome associated with isolated del(5q) (2) Velocardiofacial syndrome (2) Chromosome 17p13.1 deletion syndrome (1) Chromosome 2q32-q33 deletion syndrome (1) Chromosome 3q29 microdeletion syndrome (1) Cri-du-chat syndrome (1) Deafness-infertility syndrome (1) Hypoparathyroidism-deafness-renal disease syndrome (1) Partial deletion of the long arm of chromosome 15 (1) Trichorhinophalangeal syndrome type II (1) WAGR syndrome (1) 10p13-p14 deletion syndrome (0) 10p15 microdeletion syndrome (0)

Broader categories

Disease (618) Human disease (14) Chromosomal disorder (12) Disease of genetic or genomic mechanism (2) Disease by etiologic mechanism (0)
Trials to join now! 17 Not yet recruiting 4 Not yet finished but already full! 11 Completed 18 Terminated 1
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