Panel | Mode of inheritance | Details |
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1 panel | ||
Green in Albinism or congenital nystagmusR-numbers: R39 Signed-off version 3.0 | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Phenotypes Nystagmus 1, Congenital, X-Linked, Infantile Nystagmus, Nystagmus, infantile periodic alternating, X-linked, 310700, Nystagmus 1, congenital, X-linked, 310700, (not relevant if inheritance through paternal line) |