Encephalopathy, Ethylmalonic (EE)

Alias:
Ethylmalonic Encephalopathy
Ee
Encephalopathy, Petechiae, and Ethylmalonic Aciduria
Ethe1 Deficiency
Epema Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Encephalopathy, Ethylmalonic, also known as ethylmalonic encephalopathy, is related to acyl-coa dehydrogenase, short-chain, deficiency of and organic acidemia, and has symptoms including ataxia, seizures and abnormality of extrapyramidal motor function. An important gene associated with Encephalopathy, Ethylmalonic is ETHE1 (ETHE1 Persulfide Dioxygenase), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. Affiliated tissues include brain and skin, and related phenotypes are encephalopathy and ethylmalonic aciduria
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
<1/1000000
28
128
43

Medical Symptom

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Description
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HPO Source Accession
No data available

Gene & Mutation

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No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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