Noonan syndrome 9
Noonan syndrome that has material basis in heterozygous mutation in the SOS2 gene on chromosome 14q21
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Noonan syndrome 9
Summary
Noonan syndrome 9 is a rare disease[1].
Key Facts
- Noonan syndrome 9's instance of is recorded as rare disease[2].
- Noonan syndrome 9's instance of is recorded as class of disease[3].
- Noonan syndrome 9's subclass of is recorded as Noonan syndrome[4].
- Noonan syndrome 9's subclass of is recorded as genetic disease[5].
- Noonan syndrome 9's subclass of is recorded as autosomal dominant disease[6].
- Noonan syndrome 9's OMIM ID is recorded as 616559[7].
- Noonan syndrome 9's Disease Ontology ID is recorded as DOID:0060587[8].
- Noonan syndrome 9's genetic association is recorded as SOS2[9].
- Noonan syndrome 9's exact match is recorded as http://identifiers.org/doid/DOID:0060587[10].
- Noonan syndrome 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060587[11].
- Noonan syndrome 9's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[12].
- Noonan syndrome 9's UMLS CUI is recorded as C4225282[13].
- Noonan syndrome 9's ICD-10-CM is recorded as Q87.1[14].
- Noonan syndrome 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Noonan syndrome 9's Mondo ID is recorded as MONDO_0014691[16].
- Noonan syndrome 9's UniProt disease ID is recorded as DI-04518[17].