Noonan syndrome 4
Noonan syndrome that has material basis in heterozygous mutation in the SOS1 gene on chromosome 2p22
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Noonan syndrome 4
Summary
Noonan syndrome 4 is a rare disease[1].
Key Facts
- Noonan syndrome 4's instance of is recorded as rare disease[2].
- Noonan syndrome 4's subclass of is recorded as Noonan syndrome[3].
- Noonan syndrome 4's subclass of is recorded as genetic disease[4].
- Noonan syndrome 4's subclass of is recorded as autosomal dominant disease[5].
- Noonan syndrome 4's MeSH descriptor ID is recorded as C548082[6].
- Noonan syndrome 4's OMIM ID is recorded as 610733[7].
- Noonan syndrome 4's genetic association is recorded as SOS1[8].
- Noonan syndrome 4's exact match is recorded as http://identifiers.org/doid/DOID:0060582[9].
- Noonan syndrome 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060582[10].
- Noonan syndrome 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[11].
- Noonan syndrome 4's UMLS CUI is recorded as C1853120[12].
- Noonan syndrome 4's ICD-10-CM is recorded as Q87.1[13].
- Noonan syndrome 4's GARD rare disease ID is recorded as 10699[14].
- Noonan syndrome 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Noonan syndrome 4's Mondo ID is recorded as MONDO_0012547[16].
- Noonan syndrome 4's UniProt disease ID is recorded as DI-02074[17].