Pages that link to "Autosomal recessive"
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The following pages link to Autosomal recessive:
Displayed 100 items.
- Anemia (← links)
- Electrocardiography (← links)
- Cystinosis (← links)
- Tyrosinemia (← links)
- Cystinuria (← links)
- Abetalipoproteinemia (← links)
- Narcolepsy (← links)
- Leukocytosis (← links)
- Neuroacanthocytosis (← links)
- Splenomegaly (← links)
- Pulmonary valve stenosis (← links)
- Fibrinogen (← links)
- Myopathy (← links)
- Atransferrinemia (← links)
- Trimethylaminuria (← links)
- Beeturia (← links)
- Hemiplegia (← links)
- Ehlers-Danlos syndrome (← links)
- Congenital adrenal hyperplasia (← links)
- Charcot-Marie-Tooth Syndrome (← links)
- OMIM (← links)
- Achondrogenesis (← links)
- ICD-10 Chapter Q (← links)
- Mendelian Inheritance in Man (← links)
- ICD-10 Chapter G (← links)
- Diarrhea (← links)
- Krabbe disease (← links)
- Wiskott-Aldrich syndrome (← links)
- Jervell and Lange-Nielsen syndrome (← links)
- Farber disease (← links)
- Severe combined immunodeficiency (← links)
- Ichthyosis lamellaris (← links)
- Leukocyte adhesion deficiency (← links)
- Alexander disease (← links)
- Harlequin type ichthyosis (← links)
- Rabson-Mendenhall syndrome (← links)
- Chédiak-Higashi syndrome (← links)
- Young Simpson syndrome (← links)
- 3c syndrome (← links)
- Ablepharon macrostomia syndrome (← links)
- Achromatopsia (← links)
- Adenosine deaminase deficiency (← links)
- Aniridia (← links)
- Apparent mineralocorticoid excess (← links)
- Arginemia (← links)
- Ataxia telangiectasia (← links)
- Atelosteogenesis, type II (← links)
- Xanthelasma (← links)
- Bardet-Biedl syndrome (← links)
- Leber's congenital amaurosis (← links)
- 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)