Disease #05781 (LMPHM7 (lymphatic malformation, type 7), OMIM:617300)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	LMPHM7
Name	lymphatic malformation, type 7
OMIM ID	617300
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	EPHB4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-07-09 16:13:23 +02:00 (CEST)
Date last edited	2022-03-01 16:57:07 +01:00 (CET)

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