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

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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