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 11 - 13 of 13 in total
Gene ID Gene Symbol Description Source
9536 PTGES prostaglandin E synthase
23213 SULF1 sulfatase 1
51763 INPP5K inositol polyphosphate-5-phosphatase K
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 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

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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