developmental and epileptic encephalopathy 51

Summary
Synonym
  • DEE51
  • early infantile epileptic encephalopathy 51
Definition
A developmental and epileptic encephalopathy characterized by onset of intractable seizures and hypotonia in the first days or weeks of life and severely delayed psychomotor development that has_material_basis_in homozygous or compound heterozygous mutation in the MDH2 gene on chromosome 7q11.
Super Class
autosomal recessive disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0080433
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4191 MDH2 malate dehydrogenase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
17448 Mdh2 malate dehydrogenase 2, NAD (mitochondrial)
Displaying 1 entry
Gene ID Gene Symbol Description Source
81829 Mdh2 malate dehydrogenase 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
853777 MDH1 malate dehydrogenase MDH1
853994 MDH2 malate dehydrogenase MDH2
The Human Phenotype Ontology
Displaying entries 1 - 10 of 33 in total
HPO ID HPO Term
HP:0002151 Increased circulating lactate concentration
HP:0100660 Dyskinesia
HP:0001265 Hyporeflexia
HP:0003593 Infantile onset
HP:0000817 Reduced eye contact
HP:0002540 Inability to walk
HP:0007371 Corpus callosum atrophy
HP:0001344 Absent speech
HP:0000486 Strabismus
HP:0002421 Poor head control
Displaying 1 entry
Gene ID Gene Symbol Description
4191 MDH2 malate dehydrogenase 2

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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