Details of Disease

General Information of Disease (ID: DIS5SGZ9)

Disease Name Primary ciliary dyskinesia 28
Synonyms
ciliary dyskinesia, primary, 28; ciliary dyskinesia, primary, 28, with or without situs inversus; CILD28; SPAG1 primary ciliary dyskinesia; primary ciliary dyskinesia type 28; primary ciliary dyskinesia caused by mutation in SPAG1; primary ciliary dyskinesia 28 with or without situs inversus; ciliary dyskinesia, primary, type 28
Definition Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the SPAG1 gene.
Disease Hierarchy
DISOBC7V: Primary ciliary dyskinesia
DIS5SGZ9: Primary ciliary dyskinesia 28
Disease Identifiers
MONDO ID
MONDO_0014216
UMLS CUI
C3809706
OMIM ID
615505
MedGen ID
816036

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
SPAG1 OT29JZKW 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.