Noonan syndrome 2
Noonan syndrome that has material basis in an autosomal recessive mutation
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Noonan syndrome 2
Summary
Noonan syndrome 2 is a class of disease[1].
Key Facts
- Noonan syndrome 2's instance of is recorded as class of disease[2].
- Noonan syndrome 2's subclass of is recorded as Noonan syndrome[3].
- Noonan syndrome 2's subclass of is recorded as autosomal recessive disease[4].
- Noonan syndrome 2's MeSH descriptor ID is recorded as C548081[5].
- Noonan syndrome 2's OMIM ID is recorded as 605275[6].
- Noonan syndrome 2's Disease Ontology ID is recorded as DOID:0060580[7].
- Noonan syndrome 2's genetic association is recorded as LZTR1[8].
- Noonan syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0060580[9].
- Noonan syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060580[10].
- Noonan syndrome 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[11].
- Noonan syndrome 2's UMLS CUI is recorded as C1854469[12].
- Noonan syndrome 2's ICD-10-CM is recorded as Q87.1[13].
- Noonan syndrome 2's GARD rare disease ID is recorded as 10698[14].
- Noonan syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Noonan syndrome 2's Mondo ID is recorded as MONDO_0011531[16].
- Noonan syndrome 2's UniProt disease ID is recorded as DI-05439[17].