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Harrod syndrome
Disease Summary
Associated Targets ()
Mondo Description Harrod syndrome is characterized by the association of intellectual deficit, facial dysmorphism (a highly arched palate, pointed chin, and small mouth, hypotelorism, a long nose and large protruding ears), arachnodactyly, hypogenitalism (undescended testes and hypospadias) and failure to thrive.
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:0002601
MESH:C535635
OMIM:601095
Orphanet:2115
SCTID:716089008
UMLS:C0795970
MONDO:0010993
High level summary of knowledge for a disease, including descriptions and datasource references.