WormMine: DiseaseOntology DOID:0060786 hypomyelinating leukodystrophy Disease Ontology

Name
Disease Ontology

Identifier	Name	Description
DOID:7	disease of anatomical entity	A disease that manifests in a defined anatomical structure.
DOID:4	disease	A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:863	nervous system disease	A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.
DOID:936	brain disease	A central nervous system disease that is located_in the brain.
DOID:331	central nervous system disease	A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system.
DOID:10579	leukodystrophy	A cerebral degeneration characterized by dysfunction of the white matter of the brain.
DOID:1443	cerebral degeneration	A brain disease that is characterized by loss of structure or function of neurons, including death of neurons and loss of brain tissue.
DOID:0060786	hypomyelinating leukodystrophy	A leukodystrophy characterized by improper formation of the myelin sheath in the central nervous system resulting in T2 hyperintensity and variable T1 signal on magnetic resonance imaging.

Name	Type
HLD	synonym

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