Deafness, Autosomal Recessive 26, Modifier of (DFNB26M)

Alias:

Deafness, Nonsyndromic, Modifier 1

{deafness, Autosomal Recessive 26, Modifier of}

Deafness, Nonsyndromic, Modifier of, 1

Dfnb26, Suppressor of

Dfnb26, Modifier of

Dfnb26m

Dfnm1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 26, Modifier of, also known as deafness, nonsyndromic, modifier 1, is related to contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a and deafness, autosomal recessive 2. An important gene associated with Deafness, Autosomal Recessive 26, Modifier of is METTL13 (Methyltransferase 13, EEF1A N-Terminus And K55).

Related ID：

MALACARDS：DFN363

OMIM：605429