Structured Summary
Abstract
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.
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Synonyms
5 entry terms
- Cryptophthalmos with Other Malformations
- Cryptophthalmos-Syndactyly Syndrome
- Cryptophthalmos Syndactyly Syndrome
- Cryptophthalmos-Syndactyly Syndromes
- Syndrome, Fraser
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
do not confuse with FRASIER SYNDROME
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History Note
2011
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AMA Style
References
- National Library of Medicine. Fraser Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D058497. http://id.nlm.nih.gov/mesh/2026/D058497
- Fraser Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Fraser_syndrome
- Fraser Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q1425572