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Human Disease
hypomyelinating leukodystrophy 21
- Term ID
- DOID:0070407
- Synonyms
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- HLD21
- Definition
- A hypomyelinating leukodystrophy characterized by global developmental delay apparent from infancy with loss of motor, speech, and cognitive milestones in the first decades of life that has_material_basis_in homozygous mutation in the POLR3K gene on chromosome 16p13. https://pubmed.ncbi.nlm.nih.gov/30584594/
- References
- Ontology
- Human Disease ( DOID:0070407 )
- is a type of
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Genes Involved
Zebrafish Models