Understanding Neonatal Diabetes and DEND Syndrome disease
Diabetes Mellitus, Permanent Neonatal, 1, also known as permanent diabetes mellitus of infancy, is related to diabetes mellitus, permanent neonatal, 4 and cantu syndrome. An important gene associated with Diabetes Mellitus, Permanent Neonatal, 1 is GCK (Glucokinase), and among its related pathways/superpathways are Integration of energy ...
X-Linked Dystonia-Parkinsonism: Lifestyle Considerations disease
Dystonia 3, Torsion, X-Linked, also known as x-linked dystonia-parkinsonism, is related to dystonia 1, torsion, autosomal dominant and dystonia 12, and has symptoms including dystonia, myoclonus and torticollis. An important gene associated with Dystonia 3, Torsion, X-Linked is TAF1 (TATA-Box Binding Protein Associated Factor 1), and among ...
Hartsfield Syndrome: A Rare Neurological Disorder disease
Hartsfield Syndrome, also known as hartsfield-bixler-demyer syndrome, is related to fgfr1-related hartsfield syndrome and holoprosencephaly. An important gene associated with Hartsfield Syndrome is FGFR1 (Fibroblast Growth Factor Receptor 1). Affiliated tissues include brain, pituitary and bone, and related phenotypes are ptosis and ...
Elevate Your Olmsted Syndrome Lifestyle disease
Mutilating Palmoplantar Keratoderma with Periorificial Keratotic Plaques, also known as olmsted syndrome, is related to olmsted syndrome, x-linked and alopecia. An important gene associated with Mutilating Palmoplantar Keratoderma with Periorificial Keratotic Plaques is PERP (P53 Apoptosis Effector Related To PMP22), and among its related ...
Managing Autosomal Recessive Ichthyosis: Key Lifestyle Tips disease
Autosomal Recessive Congenital Ichthyosis, also known as lamellar ichthyosis, is related to ichthyosis, congenital, autosomal recessive 1 and ichthyosis, congenital, autosomal recessive 2. An important gene associated with Autosomal Recessive Congenital Ichthyosis is ALOX12B (Arachidonate 12-Lipoxygenase, 12R Type), and among its related ...