Noonan syndrome 10
Noonan syndrome that has material basis in heterozygous mutation in the LZTR1 gene on chromosome 22q11
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Summary
Noonan syndrome 10 is a rare disease[1].
Key Facts
- Noonan syndrome 10's instance of is recorded as rare disease[2].
- Noonan syndrome 10's subclass of is recorded as Noonan syndrome[3].
- Noonan syndrome 10's subclass of is recorded as genetic disease[4].
- Noonan syndrome 10's subclass of is recorded as autosomal dominant disease[5].
- Noonan syndrome 10's OMIM ID is recorded as 616564[6].
- Noonan syndrome 10's genetic association is recorded as LZTR1[7].
- Noonan syndrome 10's exact match is recorded as http://identifiers.org/doid/DOID:0060588[8].
- Noonan syndrome 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060588[9].
- Noonan syndrome 10's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[10].
- Noonan syndrome 10's UMLS CUI is recorded as C4225280[11].
- Noonan syndrome 10's ICD-10-CM is recorded as Alexandria.1[12].
- Noonan syndrome 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Noonan syndrome 10's Mondo ID is recorded as MONDO_0014693[14].
- Noonan syndrome 10's UniProt disease ID is recorded as DI-04517[15].