Disease #05607 (HLD14 (leukodystrophy, hypomyelinating, type 14 (HLD-14)), OMIM:617899)

Global Variome shared LOVD

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Official abbreviation	HLD14
Name	leukodystrophy, hypomyelinating, type 14 (HLD-14)
OMIM ID	617899
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	UFM1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-06-05 16:27:02 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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