CHD3 - Gene browser

CHD3

chromodomain helicase DNA binding protein 3

HCNC Approved Symbol: CHD3 (HGNC:1918)
Genomic Coordinates: 17:7,884,796 - 7,912,755 (17p13.1)
Synonyms: Mi-2a, ZFH, Mi2-ALPHA
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

28Patients

In total, 28 patients were diagnosed with a variant in the CHD3 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

028
Patient count

Global developmental delay: 10 (35.7%)
Patient Count: 10 (35.7%)
% of total patients presenting each phenotype is shown in parentheses.
10 (35.7%)
Macrocephaly: 8 (28.6%)
Patient Count: 8 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
8 (28.6%)
Intellectual disability: 6 (21.4%)
Patient Count: 6 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
6 (21.4%)
Delayed speech and language development: 4 (14.3%)
Patient Count: 4 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
4 (14.3%)
Hypertelorism: 4 (14.3%)
Patient Count: 4 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
4 (14.3%)