Disease #04636 (HLD-10 (leukodystrophy, hypomyelinating, type 10 (HLD-10)), OMIM:616420)

Official abbreviation HLD-10
Name leukodystrophy, hypomyelinating, type 10 (HLD-10)
OMIM ID 616420
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PYCR2
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited N/A