EDA - Gene browser

EDA

ectodysplasin A

HCNC Approved Symbol: EDA (HGNC:3157)
Genomic Coordinates: 23:69,616,113 - 70,039,472 (Xq13.1)
Synonyms: EDA1, XLHED, HED, XHED, ED1-A1, ED1-A2, EDA-A1, EDA-A2, ED1, EDA2, ODT1
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

17Patients

In total, 17 patients were diagnosed with a variant in the EDA gene.

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

017
Patient count

Ectodermal dysplasia: 6 (35.3%)
Patient Count: 6 (35.3%)
% of total patients presenting each phenotype is shown in parentheses.
6 (35.3%)
Dry skin: 5 (29.4%)
Patient Count: 5 (29.4%)
% of total patients presenting each phenotype is shown in parentheses.
5 (29.4%)
Anhidrosis: 4 (23.5%)
Patient Count: 4 (23.5%)
% of total patients presenting each phenotype is shown in parentheses.
4 (23.5%)
Hypodontia: 4 (23.5%)
Patient Count: 4 (23.5%)
% of total patients presenting each phenotype is shown in parentheses.
4 (23.5%)
Hypotrichosis: 4 (23.5%)
Patient Count: 4 (23.5%)
% of total patients presenting each phenotype is shown in parentheses.
4 (23.5%)