Additional Disease Briefs

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

congenital mesoblastic nephroma

Also known as: CMN, CMn, congenital mesoblastic nephroma, mesoblastic nephroma, stromal nephroma, malignant

congenital microcephaly – severe encephalopathy – progressive cerebral atrophy syndrome

Also known as: ASNSD, Asns deficiency, asparagine synthetase deficiency, congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndromeASNSD, Asns deficiency, asparagine synthetase deficiency, congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome

congenital microcephaly – severe encephalopathy – progressive cerebral atrophy syndrome

Also known as: ASNSD, Asns deficiency, asparagine synthetase deficiency, congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome

congenital microcoria

Also known as: Mcor, chromosome 13Q32 deletion syndrome, congenital miosis, microcoria, congenital, miosis, congenital, pinhole pupils

congenital microgastria

congenital mitral stenosis

Also known as: congenital mitral stenosis, congenital mitral stenosis (disease), congenital mitral valve stenosis, hereditary mitral valve stenosis

congenital mitral valve agenesis

congenital multicore myopathy with external ophthalmoplegia

Also known as: minicore myopathy, minicore myopathy with external ophthalmoplegia, minicore myopathy, antenatal onset, with arthrogryposis, multicore myopathy, multicore myopathy with external ophthalmoplegia, multiminicore disease with external ophthalmoplegia, multiminicore myopathy multicore myopathy with external ophthalmoplegia