Misplaced Pages

The following pages link to Compound heterozygosity

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• transclusion count
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Showing 50 items.

• Mutation (links | edit)
• Phenylketonuria (links | edit)
• Tay–Sachs disease (links | edit)
• Hemoglobinopathy (links | edit)
• Thalassemia (links | edit)
• Leigh syndrome (links | edit)
• Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (links | edit)
• Pyruvate kinase deficiency (links | edit)
• Hypophosphatasia (links | edit)
• Hereditary elliptocytosis (links | edit)
• Pantothenate kinase-associated neurodegeneration (links | edit)
• Beta thalassemia (links | edit)
• Lipoprotein lipase deficiency (links | edit)
• SLC22A5 (links | edit)
• Yunis–Varon syndrome (links | edit)
• Phosphoglycerate dehydrogenase (links | edit)
• Compound heterozygous (redirect page) (links | edit)
  • Protein C (links | edit)
  • Adenine phosphoribosyltransferase (links | edit)
  • Organoid (links | edit)
  • Triosephosphate isomerase deficiency (links | edit)
  • GTPBP3 (links | edit)
  • Death of Ludwig van Beethoven (links | edit)
  • Generalized arterial calcification of infancy (links | edit)
  • Combined malonic and methylmalonic aciduria (links | edit)
  • Beck–Fahrner syndrome (links | edit)
  • User:Seppi333 (links | edit)
• Compound heterozygote (redirect page) (links | edit)
  • Donohue syndrome (links | edit)
  • MUTYH-associated polyposis (links | edit)
  • User:Egeorge01/sandbox (links | edit)
• Compound heterozygotes (redirect page) (links | edit)
  • Hereditary haemochromatosis (links | edit)
  • Beta thalassemia (links | edit)
  • Frataxin (links | edit)
  • FANCA (links | edit)
  • Copper in biology (links | edit)
  • ANNOVAR (links | edit)
  • User:Enviromet/Subpage 1 Copper in health - working draft (links | edit)
• Oculocutaneous albinism type I (links | edit)
• Autosomal recessive polycystic kidney disease (links | edit)
• Sickle cell disease (links | edit)
• Genetic compound (redirect page) (links | edit)
• Genetic compounds (redirect page) (links | edit)
  • GM2-gangliosidosis, AB variant (links | edit)
  • GM2A (links | edit)
• Jalili syndrome (links | edit)
• Cerebroretinal microangiopathy with calcifications and cysts (links | edit)
• IFT140 (links | edit)
• Upshaw–Schulman syndrome (links | edit)
• Langer mesomelic dysplasia (links | edit)
• Neu–Laxova syndrome (links | edit)
• Hypotrichosis with juvenile macular dystrophy (links | edit)
• Hypodysfibrinogenemia (links | edit)
• Kenny-Caffey syndrome (links | edit)
• Dopamine transporter deficiency syndrome (links | edit)
• D-glycerate dehydrogenase deficiency (links | edit)
• Talk:Phenylketonuria (links | edit)
• Talk:Compound heterozygosity (transclusion) (links | edit)
• Talk:Hereditary haemochromatosis (links | edit)
• User:Mad Price Ball/Genetics counts (links | edit)
• User:Kazkaskazkasako/Work (links | edit)
• User:Tekivela/draft crmcc (links | edit)
• User:Merlin-UK/Books/Genetics (links | edit)
• User:Dianabuja/Books/Alleles - Breeding (links | edit)
• User:Dianabuja/Books/Genetics (links | edit)
• User:MastCell/Ignored medical articles (links | edit)
• User:MikeWaddell002/Books/Gilgamesh (links | edit)
• User:PriceDL/List of all WikiProject Medicine articles (links | edit)
• User:CFCF/sandbox/46 (links | edit)
• User:Leoleonardos/Books/Genetics (links | edit)
• Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)