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Chromosome 17 disorder

MONDO:0020583

Chromosomal disorder in which chromosome 17 is affected.

Also known as: chromosome 17 abnormality

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

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Sub-types

Charcot-Marie-Tooth disease type 1A (14) Chromosome 17p deletion (5) Hereditary neuropathy with liability to pressure palsies (3) 17q11.2 microduplication syndrome (1) Chromosome 17p13.1 deletion syndrome (1) Chromosome 17q12 deletion syndrome (1) Chromosome 17q12 duplication syndrome (1) Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome (1) Potocki-Lupski syndrome (1) Trisomy 17p (1) 17q24.2 microdeletion syndrome (0) Chromosome 17p13.3 duplication syndrome (0) Chromosome 17q11.2 deletion syndrome, 1.4Mb (0) Chromosome 17q21.31 duplication syndrome (0) Chromosome 17q23.1-q23.2 deletion syndrome (0) Distal 17p13.1 microdeletion syndrome (0) Distal 17p13.3 microdeletion syndrome (0) Distal monosomy 17q (0) Distal trisomy 17q (0) Familial clubfoot due to 17q23.1q23.2 microduplication (0)

Broader categories

Disease (680) Human disease (14) Chromosomal disorder (12) Disease of genetic or genomic mechanism (2) Autosomal anomaly (0) Disease by etiologic mechanism (0)
Trials to join now! 14 Not yet recruiting 3 Not yet finished but already full! 3 Completed 6
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