hypomyelinating leukodystrophy
Information
- Disease name
- hypomyelinating leukodystrophy
- Disease ID
- DOID:0060786
- 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." [url:https\://pubmed.ncbi.nlm.nih.gov/24916848/, url:https\://pubmed.ncbi.nlm.nih.gov/25649058/, url:https\://pubmed.ncbi.nlm.nih.gov/27234264/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
- Disase is a (Disease Ontology)
- DOID:10579
- Cross Reference ID (Disease Ontology)
- MIM:PS312080
- Exact Synonym (Disease Ontology)
- HLD