Details of Disease | DrugMAP

General Information of Disease (ID: DISDW0C2)

Disease Name	Gabriele de Vries syndrome
Synonyms	Gabriele-de Vries syndrome; GADEVS; Gabriele-De Vries syndrome; YY1 haploinsufficiency syndrome
Disease Hierarchy	DISDOXWZ: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability DISDW0C2: Gabriele de Vries syndrome
Disease Identifiers	MONDO ID MONDO_0044738 UMLS CUI C4479652 OMIM ID 617557 MedGen ID 1375401 Orphanet ID 506358 SNOMED CT ID 1186730002

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
YY1	OTYO4VOX	Strong	Autosomal dominant	[1]
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References

1	Targeted disruption of mouse Yin Yang 1 transcription factor results in peri-implantation lethality. Mol Cell Biol. 1999 Oct;19(10):7237-44. doi: 10.1128/MCB.19.10.7237.