|  Help  |  About  |  Contact Us

DO Term : hypomyelinating leukodystrophy [DOID:0060786] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • PS312080,
  • OMIM:PS312080,
  • HLD
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents