All diseases

OMIM ID
130060
OMIM term:
EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT
Alternative terms:
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE
EDS VIIA; EDS7A
ARTHROCHALASIS MULTIPLEX CONGENITA
EDS VII, MUTANT PROCOLLAGEN TYPE EDS VIIB, INCLUDED; EDS7B, INCLUDED
(∗) Location:
17q21.33   7q21.3  
(†) Associated OMIM genes:
COL1A1   COL1A2  
(‡) Associated MGI genes:

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