primary ciliary dyskinesia 6
primary ciliary dyskinesia that is characterized by partial outer dynein arm defect and has material basis in mutation in the TXNDC3 gene on the chromosome 7p14.1
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primary ciliary dyskinesia 6
Summary
primary ciliary dyskinesia 6 is a rare disease[1].
Key Facts
- primary ciliary dyskinesia 6's instance of is recorded as rare disease[2].
- primary ciliary dyskinesia 6's instance of is recorded as class of disease[3].
- primary ciliary dyskinesia 6's subclass of is recorded as primary ciliary dyskinesia[4].
- primary ciliary dyskinesia 6's MeSH descriptor ID is recorded as C567057[5].
- primary ciliary dyskinesia 6's OMIM ID is recorded as 610852[6].
- primary ciliary dyskinesia 6's Disease Ontology ID is recorded as DOID:0110606[7].
- primary ciliary dyskinesia 6's health specialty is recorded as medical genetics[8].
- primary ciliary dyskinesia 6's genetic association is recorded as NME8[9].
- primary ciliary dyskinesia 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110606[10].
- primary ciliary dyskinesia 6's exact match is recorded as http://identifiers.org/doid/DOID:0110606[11].
- primary ciliary dyskinesia 6's UMLS CUI is recorded as C1970506[12].
- primary ciliary dyskinesia 6's ICD-10-CM is recorded as Q34.8[13].
- primary ciliary dyskinesia 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- primary ciliary dyskinesia 6's Mondo ID is recorded as MONDO_0012571[15].
- primary ciliary dyskinesia 6's UniProt disease ID is recorded as DI-00931[16].