Fraser syndrome

Summary
Synonym
  • cryptophthalmos with other malformations
Definition
A syndrome characterized by cryptophthalmos, syndactyly, ambiguous genitalia, laryngeal and genitourinary malformations, oral clefting, and mental retardation that has_material_basis_in homozygous or compound heterozygous mutation in the FRAS1 gene on chromosome 4q21, the FREM2 gene on chromosome 13q13, or the GRIP1 gene on chromosome 12q14.
Super Class
autosomal recessive disease syndrome
Disease Ontology
DOID:0090001
Mondo Disease Ontology
MeSH
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
23426 GRIP1 glutamate receptor interacting protein 1
80144 FRAS1 Fraser extracellular matrix complex subunit 1
158326 FREM1 FRAS1 related extracellular matrix 1
341640 FREM2 FRAS1 related extracellular matrix 2
Displaying all 4 entries
Gene ID Gene Symbol Description Source
74053 Grip1 glutamate receptor interacting protein 1
231470 Fras1 Fraser extracellular matrix complex subunit 1
242022 Frem2 Fras1 related extracellular matrix protein 2
329872 Frem1 Fras1 related extracellular matrix protein 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024