megalencephalic leukoencephalopathy with subcortical cysts 2B

Summary
Synonym
  • megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation
Definition
A megalencephalic leukoencephalopathy with subcortical cysts characterized by infantile-onset macrocephaly and mildly delayed motor development associated with white matter abnormalities that improve with age, and sometimes mental retardation that has_material_basis_in heterozygous mutation in the HEPACAM gene on chromosome 11q24.
Super Class
autosomal dominant disease megalencephalic leukoencephalopathy with subcortical cysts
Disease Ontology
DOID:0080317
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
220296 HEPACAM hepatic and glial cell adhesion molecule
Displaying 1 entry
Gene ID Gene Symbol Description Source
72927 Hepacam hepatocyte cell adhesion molecule
The Human Phenotype Ontology
Displaying entries 1 - 10 of 22 in total
HPO ID HPO Term
HP:0001177 Preaxial hand polydactyly
HP:0002890 Thyroid carcinoma
HP:0000750 Delayed speech and language development
HP:0007018 Attention deficit hyperactivity disorder
HP:0001270 Motor delay
HP:0000316 Hypertelorism
HP:0005280 Depressed nasal bridge
HP:0001250 Seizure
HP:0200008 Intestinal polyposis
HP:0001012 Multiple lipomas
Displaying 1 entry
Gene ID Gene Symbol Description
5728 PTEN phosphatase and tensin homolog

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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