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Kenny-Caffey syndrome
Disease Summary
Associated Targets (2)
Tbio
2
Mondo Description A genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia.
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.
DC:0000549
MESH:C537020
NCIT:C130991
OMIMPS:127000
Orphanet:2333
SCTID:82837002
UMLS:C0265291
MONDO:0016516
High level summary of knowledge for a disease, including descriptions and datasource references.