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XB-GENEPAGE-944904
rp9 retinitis pigmentosa 9 (autosomal dominant)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (30 sources): Abnormal electroretinogram, Abnormal retinal vascular morphology, Abnormal testis morphology, Abnormality of fundus pigmentation, Abnormality of retinal pigmentation, Anteverted nares, Atypical scarring of skin, Blindness, Cataract, Conductive hearing impairment, [+] |
Mouse (6 sources): abnormal adipose tissue amount, abnormal body length, decreased body length, hydrometra, increased total body fat amount, small superior vagus ganglion |
View all ortholog results at Monarch |