Marinesco-Sjogren syndrome

Summary
Synonym
  • Garland-Moorhouse syndrome
  • Marinesco-Garland syndrome
  • Oligophrenic cerebellolenticular degeneration
  • hereditary oligophrenic cerebello-lental degeneration
Definition
A syndrome characterized by congenital cataracts, cerebellar ataxia, progressive muscle weakness due to myopathy, and delayed psychomotor development.
Super Class
autosomal recessive disease syndrome
Disease Ontology
DOID:0080195
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
64374 SIL1 SIL1 nucleotide exchange factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
81500 Sil1 SIL1 nucleotide exchange factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
291673 Sil1 SIL1 nucleotide exchange factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
43034 Sil1 Sil1 nucleotide exchange factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
854126 SIL1 Sil1p
The Human Phenotype Ontology
Displaying entries 1 - 10 of 43 in total
HPO ID HPO Term
HP:0000135 Hypogonadism
HP:0000252 Microcephaly
HP:0000486 Strabismus
HP:0000518 Cataract
HP:0000639 Nystagmus
HP:0000648 Optic atrophy
HP:0000768 Pectus carinatum
HP:0001156 Brachydactyly
HP:0001167 Abnormal finger morphology
HP:0001249 Intellectual disability
Displaying 1 entry
Gene ID Gene Symbol Description
51763 INPP5K inositol polyphosphate-5-phosphatase K

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024