All diseases

OMIM ID
130020
OMIM term:
EHLERS-DANLOS SYNDROME, TYPE III
Alternative terms:
EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE
EDS III
EDS3
BENIGN HYPERMOBILITY SYNDROME
(∗) Location:
2q32.2   6p21.33  
(†) Associated OMIM genes:
COL3A1   TNXB  
(‡) Associated MGI genes:

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