Noonan syndrome 5
Noonan syndrome that has material basis in mutation in the RAF1 gene
Press Enter · cited answer in seconds
0 sources
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 is a type of Noonan syndrome[4].
- Noonan syndrome 5 is a type of genetic disease[5].
- Noonan syndrome 5 is a type of autosomal dominant disease[6].
- Noonan syndrome 5's genetic association is recorded as RAF1[7].
- Noonan syndrome 5's exact match is recorded as http://identifiers.org/doid/DOID:0060583[8].
- Noonan syndrome 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060583[9].
- Noonan syndrome 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[10].
- Noonan syndrome 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].