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Chromosome 17p deletion

MONDO:0022754

A cytogenetic abnormality that refers to the allelic loss of all or part of the short arm of chromosome 17.

Also known as: chromosome 17p deletion, partial deletion of chromosome 17p, partial deletion of the short arm of chromosome 17, partial monosomy of chromosome 17p, partial monosomy of the short arm of chromosome 17, partial monosomy of the short arm of chromosome type 17, 17p deletion, 17p monosomy

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

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Sub-types

Hereditary neuropathy with liability to pressure palsies (3) Chromosome 17p13.1 deletion syndrome (1) Distal 17p13.1 microdeletion syndrome (0) Distal 17p13.3 microdeletion syndrome (0) Miller-Dieker lissencephaly syndrome (0)

Broader categories

Disease (618) Human disease (14) Chromosomal disorder (12) Disease of genetic or genomic mechanism (2) Autosomal anomaly (0) Chromosome 17 disorder (0) Disease by etiologic mechanism (0) Partial deletion of chromosome 17 (0) Syndrome caused by partial chromosomal deletion (0)
Trials to join now! 3 Not yet recruiting 1 Not yet finished but already full! 3 Completed 4
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