congenital mesoblastic nephroma
Also known as: CMN, CMn, congenital mesoblastic nephroma, mesoblastic nephroma, stromal nephroma, malignant
Additional Disease Briefs
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
congenital muscular dystrophy 1B
Also known as: CMD1B, MDC1B, congenital muscular dystrophy type 1B, muscular dystrophy, congenital, 1B
congenital muscular dystrophy due to integrin alpha-7 deficiency
Also known as: ITGA7 congenital muscular dystrophy, congenital muscular dystrophy caused by mutation in ITGA7, congenital muscular dystrophy with ITGA7 deficiency, congenital muscular dystrophy with integrin alpha-7 deficiency, congenital myopathy due to integrin alpha-7 deficiency, muscular dystrophy, congenital, due to ITGA7 deficiency, muscular dystrophy, congenital, due to integrin ALPHA-7 deficiency, myopathy, congenital, due to integrin Alpha-7 deficiency