Syndrome

Fraser Syndrome

AMW:DIS:050030

Rare autosomal recessive congenital malformation syndrome characterized by cryptophthalmos, SYNDACTYLY and UROGENITAL ABNORMALITIES. Other anomalies of bone, ear, lung, and nose are common. Mutations on FRAS1 and FREM2 are associated with the syndrome.

Pathology clinical

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Fraser Syndrome has parent Abnormalities, Multiple

Fraser Syndrome has parent Eye Abnormalities

Fraser Syndrome has parent Syndactyly

Fraser Syndrome has parent Urogenital Abnormalities

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