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XB-GENEPAGE-6468885
plekhg2 pleckstrin homology and RhoGEF domain containing G2
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (11 sources): Diffuse white matter abnormalities, Dystonia, Generalized hypotonia, Global developmental delay, Intellectual disability, severe, Leukodystrophy, Microcephaly, Nystagmus, Profound global developmental delay, Secondary microcephaly, [+] |
View all ortholog results at Monarch |