All diseases

OMIM ID
229200
OMIM term:
BRITTLE CORNEA SYNDROME 1; BCS1
Alternative terms:
FRAGILITAS OCULI WITH JOINT HYPEREXTENSIBILITY
CORNEAL FRAGILITY, KERATOGLOBUS, BLUE SCLERAE, JOINT HYPEREXTENSIBILITY
DYSGENESIS MESODERMALIS CORNEAE ET SCLERAE
EHLERS-DANLOS SYNDROME, TYPE VIB, FORMERLY; EDS6B, FORMERLY
(∗) Location:
16q24.2  
(†) Associated OMIM genes:
ZNF469  
(‡) Associated MGI genes:

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