OCM
Description
The OCM (oncomodulin) is a protein-coding gene located on chromosome 7.
OCM refers to "Observe, copy, modify," also known as "observe, imitate, modify."
OCM is also known as OCM1, OM, ONCM.
Associated Diseases
- hearing loss, autosomal recessive
- deafness, aminoglycoside-induced
- autosomal dominant nonsyndromic hearing loss 17
- autosomal dominant nonsyndromic hearing loss 7
- autosomal dominant nonsyndromic hearing loss
- autosomal recessive nonsyndromic hearing loss 1B
- autosomal dominant nonsyndromic hearing loss 2A
- hearing loss, autosomal recessive 110
- hearing loss, autosomal dominant 74
- autosomal dominant nonsyndromic hearing loss 40
- hearing loss, autosomal recessive 117
- hearing loss, autosomal dominant 83
- autosomal dominant nonsyndromic hearing loss 3B
- hearing loss, sensorineural, autosomal-mitochondrial type
