Disease #04621 (HLD-11 (leukodystrophy, hypomyelinating, type 11 (HLD-11)), OMIM:616494)

Official abbreviation HLD-11
Name leukodystrophy, hypomyelinating, type 11 (HLD-11)
OMIM ID 616494
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene POLR1C
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited N/A