Chromosome 17p deletion

rare

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

Identifiers: MONDO:0022754 Orphanet:261965
Part of: Partial deletion of chromosome 17
Also known as: 17p deletion · 17p monosomy · 17p- syndrome · chromosome 17p deletion syndrome · deletion 17p

Subtypes

Disease	ID	Subtypes	Genes
Chromosome 17p13.1 deletion syndrome	MONDO:0013415	1
Miller-Dieker lissencephaly syndrome	MONDO:0009532
Distal 17p13.3 microdeletion syndrome	MONDO:0016839
Hereditary neuropathy with liability to pressure palsies	MONDO:0008087		PMP22

Rare disease

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