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Arthrogryposis-like hand anomaly-sensorineural deafness syndrome(DA6)

MedGen UID:
350677
Concept ID:
C1862471
Disease or Syndrome
Synonyms: ARTHROGRYPOSIS AND SENSORINEURAL DEAFNESS; Arthrogryposis, distal, type 6; Arthrogryposis-like hand anomaly and sensorineural deafness; DA6; Familial hand abnormality and sensori-neural deafness
SNOMED CT: Distal arthrogryposis type 6 (720515009); Arthrogryposis-like hand anomaly and sensorineural deafness syndrome (720515009)
Modes of inheritance:
Unknown inheritance
MedGen UID:
989040
Concept ID:
CN307042
Finding
Source: Orphanet
Hereditary clinical entity whose mode of inheritance is unknown.
 
Monarch Initiative: MONDO:0007159
OMIM®: 108200
Orphanet: ORPHA1144

Definition

Distal arthrogryposis type 6 (DA6) is distinguished by the additional feature of sensorineural deafness (summary by Bamshad et al., 2009). For a phenotypic description and a discussion of genetic heterogeneity of distal arthrogryposis, see DA1 (108120). [from OMIM]

Clinical features

From HPO
Sensorineural hearing loss disorder
MedGen UID:
9164
Concept ID:
C0018784
Disease or Syndrome
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.
Arthrogryposis-like hand anomaly
MedGen UID:
870719
Concept ID:
C4025173
Congenital Abnormality
Arthrogryposis multiplex congenita
MedGen UID:
1830310
Concept ID:
C5779613
Disease or Syndrome
Multiple congenital contractures in different body areas.

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