Details of Disease | DrugMAP

General Information of Disease (ID: DISXXXWT)

Disease Name	Webb-Dattani syndrome
Synonyms	hypothalamo-pituitary-frontotemporal hypoplasia with visual and renal anomalies; WEBB-Dattani syndrome; WEDAS; hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome; Webb-Dattani syndrome
Disease Hierarchy	DISYKSRF: Genetic disease DISXXXWT: Webb-Dattani syndrome
Disease Identifiers	MONDO ID MONDO_0014404 UMLS CUI C4014708 OMIM ID 615926 MedGen ID 863145 Orphanet ID 370006

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
ARNT2	OTAQD3YV	Strong	Autosomal recessive	[1]
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References

1	Targeted mutation of the murine arylhydrocarbon receptor nuclear translocator 2 (Arnt2) gene reveals partial redundancy with Arnt. Proc Natl Acad Sci U S A. 2001 Jun 5;98(12):6692-7. doi: 10.1073/pnas.121494298. Epub 2001 May 29.