Term Name: | hypomyelinating leukodystrophy 21 |
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Synonyms: | 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. |
Ontology: | Human Disease [DOID:0070407] ( DOID:0070407 ) |