U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

MROS Melkersson-Rosenthal syndrome [ Homo sapiens (human) ]

Gene ID: 8011, updated on 31-Aug-2024

Summary

Go to the top of the page Help
Official Symbol
MROSprovided by HGNC
Official Full Name
Melkersson-Rosenthal syndromeprovided by HGNC
Primary source
MIM:155900
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MRS

Genomic context

Go to the top of the page Help
Location:
9p11

Bibliography

Go to the top of the pageHelp

Related articles in PubMed

  1. [Melkersson-Rosenthal syndrome as a rare cause of recurrent facial nerve palsy]. Opala G, et al. Neurol Neurochir Pol, 2005 Jul-Aug. PMID 16096940
  2. Melkersson-Rosenthal syndrome: new clinicopathologic findings in 4 cases. Cockerham KP, et al. Arch Ophthalmol, 2000 Feb. PMID 10676788
  3. Melkersson-Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation. Smeets E, et al. Clin Genet, 1994 Jun. PMID 7923865

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Associated conditions

Description Tests
Melkersson-Rosenthal syndrome
OMIM: 155900GeneReviews: Not available

General gene information

Go to the top of the page Help

Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases
Research Materials