atrial heart septal defect 3
atrial heart septal defect type 3 that has material basis in heterozygous mutation in the myosin heavy chain-6 gene (MYH6) on chromosome 14q12
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atrial heart septal defect 3
Summary
atrial heart septal defect 3 is a rare disease[1].
Key Facts
- atrial heart septal defect 3's instance of is recorded as rare disease[2].
- atrial heart septal defect 3's instance of is recorded as class of disease[3].
- atrial heart septal defect 3's subclass of is recorded as atrial heart septal defect[4].
- atrial heart septal defect 3's MeSH descriptor ID is recorded as C563540[5].
- atrial heart septal defect 3's OMIM ID is recorded as 614089[6].
- atrial heart septal defect 3's Disease Ontology ID is recorded as DOID:0110108[7].
- atrial heart septal defect 3's health specialty is recorded as medical genetics[8].
- atrial heart septal defect 3's genetic association is recorded as MYH6[9].
- atrial heart septal defect 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110108[10].
- atrial heart septal defect 3's exact match is recorded as http://identifiers.org/doid/DOID:0110108[11].
- atrial heart septal defect 3's UMLS CUI is recorded as C3279790[12].
- atrial heart septal defect 3's UMLS CUI is recorded as C1834527[13].
- atrial heart septal defect 3's ICD-10-CM is recorded as Q21.1[14].
- atrial heart septal defect 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- atrial heart septal defect 3's Mondo ID is recorded as MONDO_0013567[16].
- atrial heart septal defect 3's UniProt disease ID is recorded as DI-00151[17].