hypomyelinating leukodystrophy 19 (DOID:0070400)
Alliance: disease page
Synonyms: HLD19
Alt IDs: OMIM:618688
Definition: A hypomyelinating leukodystrophy characterized by onset of transient neurologic abnormalities in early infancy with resolution within the first or second decades that has_material_basis_in heterozygous mutation in the TMEM63A gene on chromosome 1q42.