Pages that link to "Autosomal recessive"
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The following pages link to Autosomal recessive:
Displayed 100 items.
- Progressive external ophthalmoplegia (← links)
- Lecithin cholesterol acyltransferase deficiency (← links)
- Retinitis pigmentosa (← links)
- Becker's muscular dystrophy (← links)
- Biotinidase deficiency (← links)
- Blue diaper syndrome (← links)
- Insulin receptor (← links)
- GABAC receptor (← links)
- GATA1 (← links)
- Familial hypercholesterolemia (← links)
- Progressive familial intrahepatic cholestasis (← links)
- Acute fatty liver of pregnancy (← links)
- Congenital hepatic fibrosis (← links)
- Autosome (← links)
- Ascertainment bias (← links)
- Genetic disorder (← links)
- Alpha 1-antitrypsin (← links)
- Factor XII (← links)
- Factor XI (← links)
- Factor V (← links)
- Leukemoid reaction (← links)
- Microcytic anemia (← links)
- Excinuclease (← links)
- 3-Methylglutaconic aciduria (← links)
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (← links)
- 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (← links)
- Abderhalden-Kaufmann-Lignac syndrome (← links)
- Adducted thumb syndrome (← links)
- Anticipation (genetics) (← links)
- Behr's syndrome (← links)
- Beta-ketothiolase deficiency (← links)
- Canavan disease (← links)
- Carbamoyl phosphate synthetase I deficiency (← links)
- Carnitine palmitoyltransferase I deficiency (← links)
- Carnitine palmitoyltransferase II deficiency (← links)
- Chronic granulomatous disease (← links)
- Citrullinemia (← links)
- Cockayne syndrome (← links)
- Coffin-Siris syndrome (← links)
- Congenital muscular dystrophy (← links)
- Congenital myopathy (← links)
- Copper toxicosis (← links)
- Dejerine Sottas syndrome (← links)
- Ellis-van Creveld syndrome (← links)
- Emery-Dreifuss muscular dystrophy (← links)
- Ethylmalonic encephalopathy (← links)
- GM2-gangliosidosis, AB variant (← links)
- Giant axonal neuropathy (← links)
- Glucose-galactose malabsorption (← links)
- Glutaric acidemia type 2 (← links)
- Glutaric aciduria type 1 (← links)
- Hereditary coproporphyria (← links)
- Holocarboxylase synthetase deficiency (← links)
- Hyper-IgE syndrome (← links)
- Hyperimmunoglobulinemia D with recurrent fever (← links)
- Hypermethioninemia (← links)
- Hyperprolinemia (← links)
- Hypomagnesemia with secondary hypocalcemia (← links)
- Infantile neuroaxonal dystrophy (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Isovaleric acidemia (← links)
- Joubert syndrome (← links)
- Lipoid congenital adrenal hyperplasia (← links)
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (← links)
- Malonyl-CoA decarboxylase deficiency (← links)
- Mitochondrial trifunctional protein deficiency (← links)
- Myotonia congenita (← links)
- Nemaline myopathy (← links)
- Nephronophthisis (← links)
- Omenn syndrome (← links)
- Ornithine translocase deficiency (← links)
- Otospondylomegaepiphyseal dysplasia (← links)
- Pendred syndrome (← links)
- Primary carnitine deficiency (← links)
- Pyruvate carboxylase deficiency (← links)
- Recessive multiple epiphyseal dysplasia (← links)
- Salla disease (← links)
- Sandhoff disease (← links)
- Sanfilippo syndrome (← links)
- Smith-Lemli-Opitz syndrome (← links)
- Spinocerebellar ataxia (← links)
- Tangier disease (← links)
- Tay-Sachs disease (← links)
- Tetrahydrobiopterin deficiency (← links)
- Usher syndrome (← links)
- Very long-chain acyl-coenzyme A dehydrogenase deficiency (← links)
- Waardenburg syndrome (← links)
- Weissenbacher-Zweymüller syndrome (← links)
- Xeroderma pigmentosum (← links)
- ZAP70 deficiency (← links)
- Zunich-Kaye syndrome (← links)
- Mucolipidosis type IV (← links)
- MUTYH (← links)
- Biotinidase (← links)
- Parkin (ligase) (← links)
- Alkaline phosphatase (← links)
- 3-hydroxy-3-methylglutaryl-CoA lyase (← links)
- Nebulin (← links)
- Methylmalonyl CoA epimerase (← links)
- Homogentisate 1,2-dioxygenase (← links)