Fraser Syndrome

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"Fraser Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D058497
MeSH Number(s)	C11.250.390 C16.131.077.371 C16.131.384.442
Concept/Terms	Fraser Syndrome Fraser Syndrome Syndrome, Fraser Cryptophthalmos with Other Malformations Cryptophthalmos-Syndactyly Syndrome Cryptophthalmos Syndactyly Syndrome Cryptophthalmos-Syndactyly Syndromes Syndrome, Cryptophthalmos-Syndactyly

Below are MeSH descriptors whose meaning is more general than "Fraser Syndrome".

Diseases [C]
Eye Diseases [C11]
Eye Abnormalities [C11.250]
Fraser Syndrome [C11.250.390]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Fraser Syndrome [C16.131.077.371]
Eye Abnormalities [C16.131.384]
Fraser Syndrome [C16.131.384.442]

Below are MeSH descriptors whose meaning is related to "Fraser Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Fraser Syndrome".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Fraser Syndrome" by people in UAMS Profiles by year, and whether "Fraser Syndrome" was a major or minor topic of these publications.

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