Related MeSH Hierarchy (12)
Diseases [C] » Musculoskeletal Diseases [C05] » Bone Diseases » Bone Diseases, Developmental » Dysostoses » Synostosis » Syndactyly » Fraser Syndrome
Diseases [C] » Musculoskeletal Diseases [C05] » Musculoskeletal Abnormalities » Limb Deformities, Congenital » Syndactyly » Fraser Syndrome
Diseases [C] » Musculoskeletal Diseases [C05] » Musculoskeletal Abnormalities » Synostosis » Syndactyly » Fraser Syndrome
Diseases [C] » Eye Diseases [C11] » Eye Abnormalities » Fraser Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Abnormalities, Multiple » Fraser Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Eye Abnormalities » Fraser Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Musculoskeletal Abnormalities » Limb Deformities, Congenital » Syndactyly » Fraser Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Musculoskeletal Abnormalities » Synostosis » Syndactyly » Fraser Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Urogenital Abnormalities » Fraser Syndrome
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urogenital Abnormalities » Fraser Syndrome
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urogenital Abnormalities » Fraser Syndrome
Diseases [C] » Urogenital Diseases [C12] » Urogenital Abnormalities » Fraser Syndrome
Description
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. MeSH
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