Details of Disease | DrugMAP

General Information of Disease (ID: DISET3W3)

Disease Name	Partial deletion of the short arm of chromosome 10
Synonyms	partial monosomy of the short arm of chromosome 10; partial deletion of chromosome 10p; partial deletion of the short arm of chromosome type 10; partial monosomy of chromosome 10p
Disease Hierarchy	: DIS1DD8C: Syndrome caused by partial chromosomal deletion DISET3W3: Partial deletion of the short arm of chromosome 10
Disease Identifiers	MONDO ID MONDO_0016892 MESH ID C538288 UMLS CUI C0795836 MedGen ID 162776 Orphanet ID 261938

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 2 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CELF2	OTLJJ4VT	Strong	Biomarker	[1]
DERL3	OTRZRT6Q	Strong	Biomarker	[2]
------------------------------------------------------------------------------------

References

1	Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.J Mol Med (Berl). 2002 Jul;80(7):431-42. doi: 10.1007/s00109-002-0331-9. Epub 2002 Apr 4.
2	A novel unbalanced whole-arm translocation der(3;10)(q10;q10) in acute monocytic leukemia.Cancer Genet Cytogenet. 2010 Jun;199(2):134-8. doi: 10.1016/j.cancergencyto.2010.02.006.