You are using an outdated browser. Please upgrade your browser to improve your experience.
Crandall syndrome
Disease Summary
Associated Targets ()
Mondo Description This syndrome is characterized by progressive sensorineural deafness, alopecia and hypogonadism with LH and GH deficiencies. It has been described in three brothers. It resembles Bjrnstad's syndrome that combines irregular pili torti and deafness. It is probably inherited as and autosomal recessive disorder.
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:0001561
Orphanet:202
SCTID:278098005
UMLS:C0432348
MONDO:0016067
High level summary of knowledge for a disease, including descriptions and datasource references.