Details of Disease | DrugMAP

General Information of Disease (ID: DISKTDLG)

Disease Name	Ciliary dyskinesia, primary, 47, and lissencephaly
Synonyms	ciliary dyskinesia, primary, 47, and lissencephaly; CILD47
Disease Hierarchy	DISOBC7V: Primary ciliary dyskinesia DISKTDLG: Ciliary dyskinesia, primary, 47, and lissencephaly
Disease Identifiers	MONDO ID MONDO_0030346 UMLS CUI C5561951 OMIM ID 619466 MedGen ID 1794161

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
TP73	OT0LUO47	Strong	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.