Disease #00106 (NFNS (NEUROFIBROMATOSIS-NOONAN SYNDROME), OMIM:601321)

Official abbreviation NFNS
Name NEUROFIBROMATOSIS-NOONAN SYNDROME
OMIM ID 601321
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NF1
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 09:47:27 +00:00 (UTC)
Date last edited N/A

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