FRAXF syndrome

MONDO:0015084

FRAXF syndrome was originally identified in a family with developmental delay and an expanded CCG repeat at the folate-sensitive FRAXF fragile site. Since this initial description, FRAXF has been associated with a range of manifestations but no clear phenotype has been established.

0 clinical trials for this condition and its sub-types, 0 tagged with FRAXF syndrome itself.

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↑ Hereditary disease (18187) ↑ Syndromic disease (7133)

Including sub-types (0) Tagged with FRAXF syndrome (0)

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