HYDIN - Gene browser

HYDIN

HYDIN axonemal central pair apparatus protein

HCNC Approved Symbol: HYDIN (HGNC:19368)
Genomic Coordinates: 16:70,802,084 - 71,230,722 (16q22.2)
Synonyms: DKFZp434D0513, KIAA1864, PPP1R31, CILD5
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

7Patients

In total, 7 patients were diagnosed with a variant in the HYDIN gene.

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

07
Patient count

Bronchiectasis: 4 (57.1%)
Patient Count: 4 (57.1%)
% of total patients presenting each phenotype is shown in parentheses.
4 (57.1%)
Aspergillus infections, recurrent: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Failure to thrive: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Immunodeficiency: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Nasal congestion: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)