Ehlers-Danlos syndrome, autosomal dominant, type unspecified
MONDO:0007528Also known as: Ehlers-Danlos syndrome, autosomal dominant, type unspecified, EDS, unspecified type, Ehlers-Danlos syndrome, Friedman-Harrod type
0 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(680)
Hereditary disease
(176)
Syndromic disease
(25)
Ehlers-Danlos syndrome
(20)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.