Noonan syndrome 3
Noonan syndrome that has material basis in heterozygous mutation in the KRAS gene
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Noonan syndrome 3
Summary
Noonan syndrome 3 is a rare disease[1].
Key Facts
- Noonan syndrome 3's instance of is recorded as rare disease[2].
- Noonan syndrome 3's subclass of is recorded as Noonan syndrome[3].
- Noonan syndrome 3's subclass of is recorded as genetic disease[4].
- Noonan syndrome 3's subclass of is recorded as autosomal dominant disease[5].
- Noonan syndrome 3's MeSH descriptor ID is recorded as C537847[6].
- Noonan syndrome 3's OMIM ID is recorded as 609942[7].
- Noonan syndrome 3's genetic association is recorded as KRAS[8].
- Noonan syndrome 3's exact match is recorded as http://identifiers.org/doid/DOID:0060581[9].
- Noonan syndrome 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060581[10].
- Noonan syndrome 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[11].
- Noonan syndrome 3's UMLS CUI is recorded as C1860991[12].
- Noonan syndrome 3's ICD-10-CM is recorded as Q87.1[13].
- Noonan syndrome 3's GARD rare disease ID is recorded as 9885[14].
- Noonan syndrome 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Noonan syndrome 3's Mondo ID is recorded as MONDO_0012371[16].
- Noonan syndrome 3's UniProt disease ID is recorded as DI-02073[17].