Disease #00018 (17-beta-hydroxysteroid dehydrogenase X deficiency, OMIM:300438)

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Official abbreviation	-
Name	17-beta-hydroxysteroid dehydrogenase X deficiency
OMIM ID	300438
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HSD17B10
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-07-23 10:50:29 +02:00 (CEST)
Date last edited	N/A