BHLHA9 - Gene browser | 3billion

BHLHA9

BHLHA9

basic helix-loop-helix family member a9

HCNC Approved Symbol: BHLHA9 (HGNC:35126)
Genomic Coordinates: 17:1,270,444 - 1,271,815 (17p13.3)
Synonyms: BHLHF42
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the BHLHA9 gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Split hand: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

BHLHA9 - Gene browser | 3billion