Disease #05167 (HMLR-1 (Heimler syndrome, type 1 (HMLR-1)), OMIM:234580)

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	Curator: Johan T. den Dunnen

Official abbreviation	HMLR-1
Name	Heimler syndrome, type 1 (HMLR-1)
OMIM ID	234580
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PEX1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-05-25 15:33:09 +02:00 (CEST)
Date last edited	N/A