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diaphragmatic hernia 3
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any congenital diaphragmatic hernia in which the cause of the disease is a mutation in the ZFPM2 gene.
Uniprot Description Form of congenital diaphragmatic hernia (CDH). CDH refers to a group of congenital defects in the structural integrity of the diaphragm associated with often lethal pulmonary hypoplasia and pulmonary hypertension.
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.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MESH:C565710
OMIM:610187
MONDO:0012431
High level summary of knowledge for a disease, including descriptions and datasource references.