HOXD13 - Gene browser

HOXD13

homeobox D13

HCNC Approved Symbol: HOXD13 (HGNC:5136)
Genomic Coordinates: 2:176,087,487 - 176,095,944 (2q31.1)
Synonyms: HOX4I, SPD
Disease Associations: This gene is associated with the following 5 diseases in OMIM.

5Patients

In total, 5 patients were diagnosed with a variant in the HOXD13 gene.

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

05
Patient count

2-3 finger syndactyly: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)
Anal atresia: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)
Bilateral palatoschisis: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)
Hydronephrosis: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)
Multicystic renal dysplasia: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)