Fraser Syndrome

"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

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

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

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PLoS One
J Med Genet
J Am Soc Nephrol
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