Fraser Syndrome
A rare, autosomal recessive inherited disorder caused by mutations in the FRAS1, FREM2, or GRIP1 genes. It is characterized by the presence of cryptophthalmos, cutaneous syndactyly, and genitourinary abnormalities.
C118436
CL479890
Cellosaurus
Cryptophthalmos-Syndactyly Syndrome
Disease or Syndrome
Fraser Syndrome
Fraser Syndrome
Cellosaurus Disease Terminology
Cellosaurus Terminology
Syndrome
Rare Non-Neoplastic Disorder