Living with Oculocutaneous Albinism Type II disease
Albinism, Oculocutaneous, Type Ii, also known as oca2, is related to skin/hair/eye pigmentation, variation in, 1 and acute contagious conjunctivitis. An important gene associated with Albinism, Oculocutaneous, Type Ii is OCA2 (OCA2 Melanosomal Transmembrane Protein), and among its related pathways/superpathways are GPR143 in melanocytes and ...
Elevate Your Postpartum Care: Mastering Lifestyle Changes disease
Postpartum Depression, also known as depression, postpartum, is related to major depressive disorder and mood disorder, and has symptoms including pelvic pain and mental and behavioral signs and symptoms. An important gene associated with Postpartum Depression is CRH (Corticotropin Releasing Hormone), and among its related ...
Gestational Trophoblastic Neoplasm: Lifestyle and Care disease
Gestational Trophoblastic Neoplasm, also known as hydatidiform mole, is related to partial hydatidiform mole and placental site trophoblastic tumor. An important gene associated with Gestational Trophoblastic Neoplasm is NLRP7 (NLR Family Pyrin Domain Containing 7), and among its related pathways/superpathways are Peptide hormone metabolism ...
Living with Split Hand-Foot Malformation disease
Split Hand-Foot Malformation, also known as ectrodactyly, is related to split-hand/foot malformation 1 and split-hand/foot malformation with long bone deficiency 1. An important gene associated with Split Hand-Foot Malformation is LEF1 (Lymphoid Enhancer Binding Factor 1), and among its related pathways/superpathways is Validated ...
Living with Chromosome 17q21.31 Deletion Syndrome disease
Koolen-De Vries Syndrome, also known as kdvs, is related to koolen-de vries syndrome due to a point mutation and hypotonia, and has symptoms including dry skin An important gene associated with Koolen-De Vries Syndrome is KANSL1 (KAT8 Regulatory NSL Complex Subunit 1), and among its related pathways/superpathways is Chromatin organization. ...