Details of Disease

General Information of Disease (ID: DISLU7XA)

Disease Name Primary ciliary dyskinesia 13
Synonyms
ciliary dyskinesia, primary, 13, with or without situs inversus; ciliary dyskinesia, primary, 13; primary ciliary dyskinesia caused by mutation in DNAAF1; ciliary dyskinesia, primary, type 13; DNAAF1 primary ciliary dyskinesia; primary ciliary dyskinesia 13; CILD13; primary ciliary dyskinesia 13 with or without situs inversus; primary ciliary dyskinesia type 13
Definition Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAAF1 gene.
Disease Hierarchy
DISOBC7V: Primary ciliary dyskinesia
DISLU7XA: Primary ciliary dyskinesia 13
Disease Identifiers
MONDO ID
MONDO_0013174
MESH ID
C567713
UMLS CUI
C2750790
OMIM ID
613193
MedGen ID
413399

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
DNAAF1 OTYLQLHO Definitive Autosomal recessive [1]
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References

1 Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.