Details of Disease | DrugMAP

General Information of Disease (ID: DISX1KHE)

Disease Name	Lacrimoauriculodentodigital syndrome 3
Disease Hierarchy	DISH8TQ5: LADD syndrome DISX1KHE: Lacrimoauriculodentodigital syndrome 3
Disease Identifiers	MONDO ID MONDO_0859578 UMLS CUI C5774287 OMIM ID 620193 MedGen ID 1824060

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
FGF10	TTNPEFX	Strong	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
FGF10	OTDSATGA	Strong	Autosomal dominant	[1]
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References

1	Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands. Nat Genet. 2005 Feb;37(2):125-7. doi: 10.1038/ng1507. Epub 2005 Jan 16.