Noonan syndrome 5
Noonan syndrome that has material basis in mutation in the RAF1 gene
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Noonan syndrome 5
Summary
Noonan syndrome 5 is a rare disease[1].
Key Facts
- Noonan syndrome 5's instance of is recorded as rare disease[2].
- Noonan syndrome 5's instance of is recorded as class of disease[3].
- Noonan syndrome 5's subclass of is recorded as Noonan syndrome[4].
- Noonan syndrome 5's subclass of is recorded as genetic disease[5].
- Noonan syndrome 5's subclass of is recorded as autosomal dominant disease[6].
- Noonan syndrome 5's MeSH descriptor ID is recorded as C548083[7].
- Noonan syndrome 5's OMIM ID is recorded as 611553[8].
- Noonan syndrome 5's Disease Ontology ID is recorded as DOID:0060583[9].
- Noonan syndrome 5's genetic association is recorded as RAF1[10].
- Noonan syndrome 5's exact match is recorded as http://identifiers.org/doid/DOID:0060583[11].
- Noonan syndrome 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060583[12].
- Noonan syndrome 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[13].
- Noonan syndrome 5's UMLS CUI is recorded as C1969057[14].
- Noonan syndrome 5's ICD-10-CM is recorded as Q87.1[15].
- Noonan syndrome 5's GARD rare disease ID is recorded as 10700[16].
- Noonan syndrome 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- Noonan syndrome 5's Mondo ID is recorded as MONDO_0012690[18].
- Noonan syndrome 5's UniProt disease ID is recorded as DI-02075[19].