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Drachtman Weinblatt Sitarz syndrome
Disease Summary
Associated Targets ()
Mondo Description A rare genetic disorder, characterized by under-development of bone marrow and neurological disorders such as weakness on one side of the body, agenesis of corpus callosum and hydrocephalus.
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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:0001913
MESH:C535603
UMLS:C2930947
MONDO:0023007
High level summary of knowledge for a disease, including descriptions and datasource references.