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Fraser Syndrome MeSH Descriptor Data 2022


MeSH Heading
Fraser Syndrome
Tree Number(s)
C05.116.099.370.894.819.428
C05.660.585.800.428
C05.660.906.819.428
C11.250.390
C12.050.351.875.397
C12.200.706.410
C12.800.410
C16.131.077.371
C16.131.384.442
C16.131.621.585.800.428
C16.131.621.906.819.428
C16.131.939.410
Unique ID
D058497
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D058497
Annotation
do not confuse with FRASIER SYNDROME
Scope Note
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.
Entry Term(s)
Cryptophthalmos with Other Malformations
Cryptophthalmos-Syndactyly Syndrome
See Also
Frasier Syndrome
Public MeSH Note
2011
History Note
2011
Date Established
2011/01/01
Date of Entry
2010/06/25
Revision Date
2021/06/30
Fraser Syndrome Preferred
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