DISEASES

Disease-gene associations mined from literature

Literature associating USH2A and retinal disease

USH2A [ENSP00000305941]

Usher syndrome 2A (autosomal recessive, mild); Involved in hearing and vision; Fibronectin type III domain containing

Synonyms:  USH2A,  USH2Ap,  hUSH2A,  O75445,  USH2A-001 ...

Linkouts:  STRING  Pharos  UniProt  OMIM