Disease #03621 (HLD8 (leukodystrophy, hypomyelinating, type 8, with/without oligodontia and/or hypogonadotropic hypogonadism (HLD8)), OMIM:614381)

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Official abbreviation	HLD8
Name	leukodystrophy, hypomyelinating, type 8, with/without oligodontia and/or hypogonadotropic hypogonadism (HLD8)
OMIM ID	614381
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	POLR3B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-01-15 19:29:15 +01:00 (CET)

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