Tyrosinemia Type I: Symptoms and Lifestyle Management disease
Tyrosinemia, Type I, also known as tyrosinemia type i, is related to glycine n-methyltransferase deficiency and abdominal obesity-metabolic syndrome 1. An important gene associated with Tyrosinemia, Type I is FAH (Fumarylacetoacetate Hydrolase), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs ...
Understanding Holoprosencephaly: Symptoms and Lifestyle Adjustments disease
Holoprosencephaly, also known as holoprosencephaly sequence, is related to holoprosencephaly 9 and holoprosencephaly 7. An important gene associated with Holoprosencephaly is FGFR1 (Fibroblast Growth Factor Receptor 1), and among its related pathways/superpathways are Signal Transduction and Signaling by Hedgehog. Affiliated tissues include ...
Elevating Your Metatropic Dysplasia Care: Lifestyle Optimization disease
Metatropic Dysplasia, also known as metatropic dwarfism, is related to spondyloepiphyseal dysplasia, maroteaux type and hereditary motor and sensory neuropathy, type iic. An important gene associated with Metatropic Dysplasia is TRPV4 (Transient Receptor Potential Cation Channel Subfamily V Member 4), and among its related ...
Elevating Your LGL Leukemia Care: Lifestyle Interventions disease
T-Cell Large Granular Lymphocyte Leukemia, also known as proliferation of large granular lymphocytes, is related to lymphoproliferative syndrome and prolymphocytic leukemia. An important gene associated with T-Cell Large Granular Lymphocyte Leukemia is STAT3 (Signal Transducer And Activator Of Transcription 3), and among its related ...
Living with INAD: Managing Life and Health disease
Neurodegeneration with Brain Iron Accumulation 2a, also known as infantile neuroaxonal dystrophy, is related to dementia, lewy body and parkinson disease 3, autosomal dominant, and has symptoms including ataxia, seizures and abnormal pyramidal signs. An important gene associated with Neurodegeneration with Brain Iron Accumulation 2a is ...