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, 6 tagged with Chromosome 17p deletion itself.

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Where it sits in the disease tree

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Part of

↑ Partial deletion of chromosome 17 (12)

Sub-types of Chromosome 17p deletion

Hereditary neuropathy with liability to pressure palsies 4 trials
Chromosome 17p13.1 deletion syndrome 1 trial
1 sub-type
- Distal 17p13.1 microdeletion syndrome 0 trials
Miller-Dieker lissencephaly syndrome 0 trials
Distal 17p13.3 microdeletion syndrome 0 trials

Including sub-types (11) Tagged with Chromosome 17p deletion (6)

Trials to join now! 3 Not yet recruiting 1 Not yet finished but already full! 4 Completed 3

Chromosome 17p deletion

Where it sits in the disease tree

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