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ENKid Syndrome
Alias:
Senter Syndrome
Keratitis-Ichthyosis-Hearing Loss/hystrix-Like Ichthyosis-Hearing Loss Syndrome
Keratitis-Ichthyosis-Deafness/hystrix-Like Ichthyosis-Deafness Syndrome
Ichthyosis Hystrix Rheydt Type
Kid/hid Syndrome
Keratitis-Ichthyosis-Deafness Syndrome
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Kid Syndrome, also known as senter syndrome, is related to keratitis, hereditary and ichthyosis, and has symptoms including photophobia An important gene associated with Kid Syndrome is GJB2 (Gap Junction Protein Beta 2), and among its related pathways/superpathways are G-protein signaling G-Protein alpha-i signaling cascades and Myometrial relaxation and contraction pathways. Affiliated tissues include skin and eye, and related phenotypes are corneal neovascularization and abnormality of the dentition
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MALACARDS
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