Search
Descriptor English: Fraser Syndrome
Descriptor Spanish: Síndrome de Fraser
Descriptor síndrome de Fraser
Scope note: Síndrome congénito malformativo, autosómico recesivo poco frecuente, caracterizado por criptoftalmos, SINDACTILIA y ANOMALÍAS GENITOURINARIAS. Son frecuentes otras anomalías óseas, del oído, pulmón y nariz. El síndrome se asocia a mutaciones de FRAS1 y FREM2.
Descriptor Portuguese: Síndrome de Fraser
Descriptor French: Syndrome de Fraser
Entry term(s): Cryptophthalmos Syndactyly Syndrome
Cryptophthalmos with Other Malformations
Cryptophthalmos-Syndactyly Syndrome
Cryptophthalmos-Syndactyly Syndromes
Syndrome, Fraser
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
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D058497
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.
Annotation: do not confuse with FRASIER SYNDROME
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 2011
History Note: 2011
Related: Frasier Syndrome MeSH
DeCS ID: 53969
Unique ID: D058497
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2011/01/01
Date of Entry: 2010/06/25
Revision Date: 2016/02/26
Fraser Syndrome - Preferred
Concept UI M0542891
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.
Preferred term Fraser Syndrome
Entry term(s) Cryptophthalmos Syndactyly Syndrome
Cryptophthalmos with Other Malformations
Cryptophthalmos-Syndactyly Syndrome
Cryptophthalmos-Syndactyly Syndromes
Syndrome, Fraser



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.


Go to survey