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acropectoral syndrome
Disease Summary
Associated Targets ()
Mondo Description Acro-pectoral syndrome is characterized by a combination of distal limb abnormalities (syndactyly of all fingers and toes, preaxial polydactyly in the feet and/or hands) and upper sternum malformations. It has been described in 22 patients from a six-generation Turkish family. It is transmitted as an autosomal dominant trait and the causative gene is located at 7q36.
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.
GARD:0008485
MESH:C535664
OMIM:605967
Orphanet:85203
SCTID:720412009
UMLS:C1853812
MONDO:0011621
High level summary of knowledge for a disease, including descriptions and datasource references.