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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.
Mondo Term and Equivalent IDs
MONDO:0016067:  Crandall syndrome
GARD:0001561: 
Orphanet:202: 
SCTID:278098005: 
UMLS:C0432348: