Details of Disease

General Information of Disease (ID: DISDJXKJ)

Disease Name Encephalomalacia
Definition Localized atrophy of the brain parenchyma due to aging, hemorrhage, infarct, or inflammation.
Disease Hierarchy
DIS6ZC3X: Brain disease
DISDJXKJ: Encephalomalacia
Disease Identifiers
MONDO ID
MONDO_0006741
MESH ID
D004678
UMLS CUI
C0014068
MedGen ID
4936
HPO ID
HP:0040197
SNOMED CT ID
58762006

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
CEBPZ OT11BATG Strong Biomarker [1]
SUOX OTEJQ9FC Strong Biomarker [2]
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References

1 Vascular Abnormalities within Normal Appearing Tissue in Chronic Traumatic Brain Injury.J Neurotrauma. 2018 Oct 1;35(19):2250-2258. doi: 10.1089/neu.2018.5684. Epub 2018 Jun 7.
2 Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.Brain Dev. 2010 Aug;32(7):544-9. doi: 10.1016/j.braindev.2009.09.005. Epub 2009 Sep 29.