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DOORS syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description DOORS syndrome (also known as DOOR syndrome) is a multiple congenital anomalies-intellectual disability syndrome characterized by sensorineural hearing loss (deafness), onychodystrophy, osteodystrophy, mild to profound intellectual disability, and seizures. Isolated seizure disorders and isolated hearing loss have also been reported in individuals as a proposed spectrum of DOORS syndrome.
Uniprot Description A syndrome characterized by sensorineural deafness, mental retardation, hypoplastic or absent nails, small or absent distal phalanges of hands and feet. Additional features include coarse facies, a large nose with wide nasal bridge, bulbous tip and anteverted nares, a long prominent philtrum and downturned corners of the mouth. Progressive neurological manifestations include seizures from infancy, optic atrophy, and peripheral polyneuropathy.
Mondo Term and Equivalent IDs
MONDO:0009079:  DOORS syndrome
DOID:0111627: 
GARD:0001685: 
MESH:C563052: 
Orphanet:79500: 
SCTID:719800009: