Additional Disease Briefs

congenital laryngeal web

Also known as: Laryngeal web, gay Feinmesser Cohen syndrome, glottic web, congenital anterior, laryngeal web, congenital heart disease and low stature, laryngeal web, familial, subglottic Bar, subglottic bar, congenital heart disease and low stature, subglottic web

congenital laryngomalacia

Also known as: congenital laryngeal stridor, laryngomalacia, laryngomalacia congenital

congenital lethal erythroderma

Also known as: congenital exfoliative erythroderma resistant to treatment, erythroderma lethal congenital, erythroderma, lethal congenital, lethal congenital erythroderma

congenital lipoid adrenal hyperplasia due to STAR deficency

Also known as: CLAH, LCAH, adrenal hyperplasia 1, congenital adrenal hyperplasia lipoid, lipoid adrenal hyperplasia, lipoid congenital adrenal hyperplasia, lipoid hyperplasia, congenital, of adrenal cortex with Male pseudohermaphroditism

congenital macroglossia

Also known as: macroglossia

congenital malabsorptive diarrhea 4

Also known as: DIAR4, NEUROG3 congenital diarrhea, NEUROG3 congenital diarrhoea, congenital diarrhea caused by mutation in NEUROG3, congenital diarrhoea caused by mutation in NEUROG3, congenital malabsorptive diarrhea due to paucity of enteroendocrine cells, congenital malabsorptive diarrhea type 4, congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells, congenital malabsorptive diarrhoea type 4, diarrhea 4, malabsorptive, congenital, diarrhoea 4, malabsorptive, congenital, enteric anendocrinosis

congenital megacalycosis

congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization

Also known as: FMAIG, alloimmune neonatal renal disease, fetomaternal alloimmunization with antenatal glomerulopathies, neonatal glomerulopathy due to Neprilysin alloimmunization, neonatal glomerulopathy due to neprilysin alloimmunization, neonatal membranous glomerulopathy with maternal NEP deficiency, neonatal membranous glomerulopathy with maternal neutral endopeptidase deficiency

congenital merosin-deficient muscular dystrophy 1A

Also known as: CMD1A, LAMA2 congenital muscular dystrophy, LAMA2-related muscular dystrophy, MDC1A, congenital merosin-deficient muscular dystrophy type 1A, congenital muscular dystrophy caused by mutation in LAMA2, congenital muscular dystrophy due to laminin alpha2 deficiency, congenital muscular dystrophy type 1A, laminin alpha-2 deficiency, merosin-deficient congenital muscular dystrophy, merosin-deficient congenital muscular dystrophy type 1A, merosin-negative congenital muscular dystrophy, muscular dystrophy, congenital merosin-deficient, muscular dystrophy, congenital merosin-deficient, 1A, muscular dystrophy, congenital merosin-deficient, type 1A, muscular dystrophy, congenital, due to partial LAMA2 deficiency, muscular dystrophy, congenital, merosin deficient or partially deficient, muscular dystrophy, congenital, merosin-deficient