Disease #02003 (HLD-3 (leukodystrophy, hypomyelinating, type 3 (HLD-3)), OMIM:260600)

Official abbreviation HLD-3
Name leukodystrophy, hypomyelinating, type 3 (HLD-3)
OMIM ID 260600
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene AIMP1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A