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LRMDA

leucine rich melanocyte differentiation associated

HCNC Approved Symbol
LRMDA (HGNC:23405)
Genomic Coordinates
10:75,431,624 - 76,560,168 (10q22.2-q22.3)
Synonyms
CDA017, OCA7, C10orf11
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the LRMDA gene.

Frequently observed phenotypes

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

Foveal hypoplasia
 1 (100.0%)
LRMDA - Gene browser | 3billion