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1p21.3 microdeletion syndrome
Disease Summary
Associated Targets (1)
Tclin
1
Mondo Description 1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:293948
SCTID:719600006
UMLS:C4304578
UMLS:CN203152
MONDO:0017405
High level summary of knowledge for a disease, including descriptions and datasource references.