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ENSeckel Syndrome 7 (SCKL7)
Alias:
Sckl7
Microcephalic Primordial Dwarfism, Dauber Type
Seckel Syndrome, Type 7
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Seckel Syndrome 7, also known as sckl7, is related to orofaciodigital syndrome i and cone-rod dystrophy 20, and has symptoms including seizures An important gene associated with Seckel Syndrome 7 is NIN (Ninein), and among its related pathways/superpathways are Organelle biogenesis and maintenance and Ciliopathies. Affiliated tissues include breast and uterus, and related phenotypes are seizure and global developmental delay
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