Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4212
Gene Symbol: MEIS2
MEIS2
CUI: C4225666
Disease: CHROMOSOME 15q14 DELETION SYNDROME
CHROMOSOME 15q14 DELETION SYNDROME 		0.300 ChromosomalRearrangement ORPHANET Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability. 24678003

2014
Entrez Id: 4212
Gene Symbol: MEIS2
MEIS2
CUI: C4225666
Disease: CHROMOSOME 15q14 DELETION SYNDROME
CHROMOSOME 15q14 DELETION SYNDROME 		0.300 ChromosomalRearrangement ORPHANET Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome. 21504564

2011
Entrez Id: 4212
Gene Symbol: MEIS2
MEIS2
CUI: C4225666
Disease: CHROMOSOME 15q14 DELETION SYNDROME
CHROMOSOME 15q14 DELETION SYNDROME 		0.300 ChromosomalRearrangement ORPHANET Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septum. 20425846

2010
Entrez Id: 4212
Gene Symbol: MEIS2
MEIS2
CUI: C4225666
Disease: CHROMOSOME 15q14 DELETION SYNDROME
CHROMOSOME 15q14 DELETION SYNDROME 		0.300 ChromosomalRearrangement ORPHANET 15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization. 18561338

2008
Entrez Id: 4212
Gene Symbol: MEIS2
MEIS2
CUI: C4225666
Disease: CHROMOSOME 15q14 DELETION SYNDROME
CHROMOSOME 15q14 DELETION SYNDROME 		0.300 ChromosomalRearrangement ORPHANET A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay. 18458017

2008
Entrez Id: 4212
Gene Symbol: MEIS2
MEIS2
CUI: C4225666
Disease: CHROMOSOME 15q14 DELETION SYNDROME
CHROMOSOME 15q14 DELETION SYNDROME 		0.300 ChromosomalRearrangement ORPHANET "Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome ""tiling path"" BAC array in a girl with heart defect, cleft palate, and developmental delay." 17163532

2007