RS2534413642 COL11A2
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Associated Conditions
Fibrochondrogenesis 2
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Autosomal recessive nonsyndromic hearing loss 53
Autosomal dominant nonsyndromic hearing loss 13
autosomal dominant
Fibrochondrogenesis 2
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Autosomal recessive nonsyndromic hearing loss 53
Autosomal dominant nonsyndromic hearing loss 13
autosomal dominant
Other Variants in COL11A2