hypomyelinating leukodystrophy Disease Ontology Browser

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Disease Ontology Browser

hypomyelinating leukodystrophy (DOID:0060786)
Alliance: disease page
Synonyms: HLD
Alt IDs: OMIM:PS312080
Definition: 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.

Disease References using Mouse Models (14)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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