Managing Hyperlipoproteinemia Type V: Lifestyle and Dietary Tips disease
Hyperlipoproteinemia, Type V, also known as hyperlipoproteinemia type v, is related to apolipoprotein c-ii deficiency and xanthomatosis, and has symptoms including hypertriglyceridemic waist An important gene associated with Hyperlipoproteinemia, Type V is APOA5 (Apolipoprotein A5), and among its related pathways/superpathways are Metabolism ...
Elevate Your Trigonocephaly Care: Lifestyle Tips disease
C Syndrome, also known as opitz trigonocephaly syndrome, is related to mucopolysaccharidosis, type ii and mucopolysaccharidosis-plus syndrome, and has symptoms including seizures An important gene associated with C Syndrome is CD96 (CD96 Molecule), and among its related pathways/superpathways are "Plasma lipoprotein assembly, remodeling, and ...
NEDCHF: Symptoms, Care, and Safety disease
Neurodevelopmental Disorder with Central Hypotonia and Dysmorphic Facies, is also known as nedchf. An important gene associated with Neurodevelopmental Disorder with Central Hypotonia and Dysmorphic Facies is HDAC4 (Histone Deacetylase 4). Affiliated tissues include brain, and related phenotypes are sleep disturbance and scoliosis
Clouston Syndrome: Genetic Skin Disorder Overview disease
Clouston Syndrome, also known as ectodermal dysplasia 2, clouston type, is related to ectodermal dysplasia 1, hypohidrotic, x-linked and cleft lip/palate, and has symptoms including photophobia An important gene associated with Clouston Syndrome is GJB6 (Gap Junction Protein Beta 6), and among its related pathways/superpathways are ...
Smith-Kingsmore Syndrome: A Rare Genetic Disorder disease
Smith-Kingsmore Syndrome, also known as macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome, is related to alacrima, achalasia, and mental retardation syndrome and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Smith-Kingsmore Syndrome is MTOR ...