Jalili syndrome

MONDO:0009007

Jalili syndrome is characterized by the association of amelogenesis imperfecta (AI) and cone-rod retinal dystrophy (CORD).

Also known as: Jalili syndrome, cone rod dystrophy-amelogenesis imperfecta syndrome, cone-rod dystrophy amelogenesis imperfecta, cone-rod dystrophy and amelogenesis imperfecta, cone-rod dystrophy with amelogenesis imperfecta

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

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↑ Hereditary disease (18187) ↑ Disorder of development or morphogenesis (5170)

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

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