Noonan syndrome 7
Noonan syndrome that has material basis in heterozygous mutation in the BRAF gene
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Noonan syndrome 7
Summary
Noonan syndrome 7 is a rare disease[1].
Key Facts
- Noonan syndrome 7's instance of is recorded as rare disease[2].
- Noonan syndrome 7's subclass of is recorded as Noonan syndrome[3].
- Noonan syndrome 7's OMIM ID is recorded as 613706[4].
- Noonan syndrome 7's genetic association is recorded as BRAF[5].
- Noonan syndrome 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[6].
- Noonan syndrome 7's UMLS CUI is recorded as C3150970[7].
- Noonan syndrome 7's ICD-10-CM is recorded as Q87.1[8].
- Noonan syndrome 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].
- Noonan syndrome 7's Mondo ID is recorded as MONDO_0013379[10].
- Noonan syndrome 7's UniProt disease ID is recorded as DI-02990[11].