Noonan syndrome 6
Noonan syndrome that has material basis in heterozygous mutation in the NRAS gene on chromosome 1p13
Press Enter · cited answer in seconds
0 sources
Noonan syndrome 6
Summary
Noonan syndrome 6 is a rare disease[1].
Key Facts
- Noonan syndrome 6's instance of is recorded as rare disease[2].
- Noonan syndrome 6's instance of is recorded as class of disease[3].
- Noonan syndrome 6's subclass of is recorded as Noonan syndrome[4].
- Noonan syndrome 6's subclass of is recorded as autosomal dominant disease[5].
- Noonan syndrome 6's MeSH descriptor ID is recorded as C548084[6].
- Noonan syndrome 6's OMIM ID is recorded as 613224[7].
- Noonan syndrome 6's Disease Ontology ID is recorded as DOID:0060584[8].
- Noonan syndrome 6's genetic association is recorded as NRAS[9].
- Noonan syndrome 6's exact match is recorded as http://identifiers.org/doid/DOID:0060584[10].
- Noonan syndrome 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060584[11].
- Noonan syndrome 6's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[12].
- Noonan syndrome 6's UMLS CUI is recorded as C2750732[13].
- Noonan syndrome 6's ICD-10-CM is recorded as Q87.1[14].
- Noonan syndrome 6's GARD rare disease ID is recorded as 10701[15].
- Noonan syndrome 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Noonan syndrome 6's Mondo ID is recorded as MONDO_0013186[17].
- Noonan syndrome 6's UniProt disease ID is recorded as DI-02558[18].