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XB-GENEPAGE-5879909
nop56 NOP56 ribonucleoprotein
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (37 sources): Ataxia, Attention deficit hyperactivity disorder, Babinski sign, Blurred vision, Bowel incontinence, Cerebellar atrophy, Difficulty walking, Diplopia, Dysarthria, Dysmetria, [+] |
View all ortholog results at Monarch |