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CHD1

chromodomain helicase DNA binding protein 1

HCNC Approved Symbol
CHD1 (HGNC:1915)
Genomic Coordinates
5:98,853,985 - 98,929,007 (5q15-q21.1)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the CHD1 gene.

Frequently observed phenotypes

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

Facial dysmorphic features are mild
 1 (100.0%)
Immunodeficiency
 1 (100.0%)
Prematurity
 1 (100.0%)
Respiratory distress
 1 (100.0%)
Respiratory problem
 1 (100.0%)
CHD1 - Gene browser | 3billion