Disease #00195 (NS8 (NOONAN SYNDROME 8), OMIM:615355)

Official abbreviation NS8
Name NOONAN SYNDROME 8
OMIM ID 615355
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene RIT1
Associated tissues -
Disease features -
Remarks -
Date created 2023-07-18 13:07:18 +00:00 (UTC)
Date last edited N/A

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