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DOID:0060786 - hypomyelinating leukodystrophy
Disease Ontology Definition:A leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system.
Synonyms: HLD,
Echinobase Genes : polr3a, hspd1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
leukodystrophy (is_a)