Disease #00152 (LDS3 (LOEYS-DIETZ SYNDROME 3), OMIM:613795)

Official abbreviation LDS3
Name LOEYS-DIETZ SYNDROME 3
OMIM ID 613795
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SMAD3
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-27 09:10:27 +00:00 (UTC)
Date last edited N/A

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