LMX1A - Gene browser

LMX1A

LIM homeobox transcription factor 1 alpha

HCNC Approved Symbol: LMX1A (HGNC:6653)
Genomic Coordinates: 1:165,201,867 - 165,356,715 (1q23.3)
Synonyms: LMX1.1, LMX1
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 LMX1A gene.

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

07
Patient count

Hearing loss: 7 (100.0%)
Patient Count: 7 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
7 (100.0%)
Hearing impairment: 4 (57.1%)
Patient Count: 4 (57.1%)
% of total patients presenting each phenotype is shown in parentheses.
4 (57.1%)
Dizziness: 1 (14.3%)
Patient Count: 1 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (14.3%)
Vertigo: 1 (14.3%)
Patient Count: 1 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (14.3%)
Progressive hearing impairment: 1 (14.3%)
Patient Count: 1 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (14.3%)