Noonan syndrome 8
Noonan syndrome that has material basis in aused by heterozygous mutation in the RIT1 gene on chromosome 1q22
Press Enter · cited answer in seconds
0 sources
Noonan syndrome 8
Summary
Noonan syndrome 8 is a rare disease[1].
Key Facts
- Noonan syndrome 8's instance of is recorded as rare disease[2].
- Noonan syndrome 8's instance of is recorded as class of disease[3].
- Noonan syndrome 8's subclass of is recorded as Noonan syndrome[4].
- Noonan syndrome 8's subclass of is recorded as genetic disease[5].
- Noonan syndrome 8's subclass of is recorded as autosomal dominant disease[6].
- Noonan syndrome 8's OMIM ID is recorded as 615355[7].
- Noonan syndrome 8's Disease Ontology ID is recorded as DOID:0060586[8].
- Noonan syndrome 8's genetic association is recorded as RIT1[9].
- Noonan syndrome 8's exact match is recorded as http://identifiers.org/doid/DOID:0060586[10].
- Noonan syndrome 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060586[11].
- Noonan syndrome 8's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[12].
- Noonan syndrome 8's UMLS CUI is recorded as C3809233[13].
- Noonan syndrome 8's ICD-10-CM is recorded as Q87.1[14].
- Noonan syndrome 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Noonan syndrome 8's Mondo ID is recorded as MONDO_0014143[16].
- Noonan syndrome 8's UniProt disease ID is recorded as DI-03849[17].