COL1A2-related Ehlers-Danlos syndrome
MONDO:0100606Any Ehler-Danlos syndrome caused by any variant in the COL1A2 gene.
0 clinical trials for this condition and its sub-types.
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Broader categories
Disease
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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
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Disease by etiologic mechanism
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