Disease #00116 (LPRD1 (LEOPARD SYNDROME 1), OMIM:151100)

Official abbreviation LPRD1
Name LEOPARD SYNDROME 1
OMIM ID 151100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PTPN11
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 10:00:30 +00:00 (UTC)
Date last edited N/A

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