Disease #00150 (MYHRS (MYHRE SYNDROME), OMIM:139210)

Official abbreviation MYHRS
Name MYHRE SYNDROME
OMIM ID 139210
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SMAD4
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-27 09:06:18 +00:00 (UTC)
Date last edited N/A

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