Details of Disease | DrugMAP

General Information of Disease (ID: DISDIJ5P)

Disease Name	Hydrocephalus, congenital communicating, 1
Synonyms	HYDCC1; HYDROCEPHALUS, CONGENITAL COMMUNICATING, 1
Disease Hierarchy	DISYKSRF: Genetic disease DISDIJ5P: Hydrocephalus, congenital communicating, 1
Disease Identifiers	MONDO ID MONDO_0032862 UMLS CUI C5231454 OMIM ID 618667 MedGen ID 1684770

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
TRIM71	OTH8UB6H	Strong	Autosomal dominant	[1]
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References

1	The let-7 microRNA target gene, Mlin41/Trim71 is required for mouse embryonic survival and neural tube closure. Cell Cycle. 2008 Dec 15;7(24):3935-42. doi: 10.4161/cc.7.24.7397. Epub 2008 Dec 13.