Disease #06903 (LMPHM10 (lymphatic malformation, type 10), OMIM:619369)

Official abbreviation LMPHM10
Name lymphatic malformation, type 10
OMIM ID 619369
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ANGPT2
Associated tissues -
Disease features -
Remarks -
Date created 2022-03-21 10:04:34 +01:00 (CET)
Date last edited N/A

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