Details of Disease

General Information of Disease (ID: DISGBMVX)

Disease Name Primary ciliary dyskinesia 22
Synonyms
ciliary dyskinesia, primary, 22, with or without situs inversus; ciliary dyskinesia, primary, 22; ciliary dyskinesia, primary, type 22; ZMYND10 primary ciliary dyskinesia; primary ciliary dyskinesia type 22; primary ciliary dyskinesia caused by mutation in ZMYND10; CILD22; primary ciliary dyskinesia 22 with or without situs inversus
Definition Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the ZMYND10 gene.
Disease Hierarchy
DISOBC7V: Primary ciliary dyskinesia
DISGBMVX: Primary ciliary dyskinesia 22
Disease Identifiers
MONDO ID
MONDO_0014192
UMLS CUI
C3809543
OMIM ID
615444
MedGen ID
815873

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
ZMYND10 OT30KEZZ 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.