Disease & disorder
partial deletion of the long arm of chromosome 13
MONDO:0016911
A cytogenetic abnormality that refers to the allelic loss of all or part of the long arm of chromosome 13.
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to partial deletion of the long arm of chromosome 13. Results are keyword matches, not yet verified disease-to-outbreak relationships.
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Background context
Partial monosomy 13q
Partial monosomy of chromosome 13q is a monosomy that results from the loss of all or part of the long arm of chromosome 13 in human beings. It is a rare genetic disorder which results in severe congenital abnormalities which are frequently fatal at an early age. Up until 2003, more than 125 cases had been documented in medical literature.
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.