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
External Links
Disease Ontology
DOID:0080195
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying entries 1 - 10 of 13 in total
Gene ID Gene Symbol Description Source
142 PARP1 poly(ADP-ribose) polymerase 1
1048 CEACAM5 CEA cell adhesion molecule 5
2194 FASN fatty acid synthase
3418 IDH2 isocitrate dehydrogenase (NADP(+)) 2
4360 MRC1 mannose receptor C-type 1
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5728 PTEN phosphatase and tensin homolog
5743 PTGS2 prostaglandin-endoperoxide synthase 2
7412 VCAM1 vascular cell adhesion molecule 1
8930 MBD4 methyl-CpG binding domain 4, DNA glycosylase
Related Glycoprotein
Displaying entry 11 - 11 of 11 in total
UniProt ID Protein Name Source
Q8IWU6 Extracellular sulfatase Sulf-1
The Human Phenotype Ontology
Displaying entries 31 - 40 of 43 in total
HPO ID HPO Term
HP:0003202 Skeletal muscle atrophy
HP:0003241 External genital hypoplasia
HP:0003510 Severe short stature
HP:0003552 Muscle stiffness
HP:0003560 Muscular dystrophy
HP:0004279 Short palm
HP:0005743 Avascular necrosis of the capital femoral epiphysis
HP:0005916 Abnormal metacarpal morphology
HP:0009830 Peripheral neuropathy
HP:0010508 Metatarsus valgus
Displaying 1 entry
Gene ID Gene Symbol Description
51763 INPP5K inositol polyphosphate-5-phosphatase K

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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: August 19, 2024