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Metadata
ID	DOID:0060790
Name	hypomyelinating leukodystrophy 3
Definition	A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of early infantile onset of global developmental delay, lack of development, lack of speech acquisition, and peripheral spasticity associated with decreased myelination in the central nervous system that has_material_basis_in homozygous mutation in the AIMP1 gene on chromosome 4q24. https://www.ncbi.nlm.nih.gov/pubmed/21092922, https://www.ncbi.nlm.nih.gov/pubmed/24958424
Xrefs	ICD10CM:E75.2 OMIM:260600 ORDO:280293
Subsets	DO_rare_slim
Synonyms	HLD3 [EXACT] Pelizaeus-Merzbacher-like disease due to AIMP1 mutation [EXACT]
Parent Relationships	is_a hypomyelinating leukodystrophy is_a autosomal recessive disease