Pages that link to "Autosomal recessive"
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The following pages link to Autosomal recessive:
Displayed 250 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)
- 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)
- Iduronidase (← links)
- Methylmalonyl-CoA mutase (← links)
- Uroporphyrinogen III synthase (← links)
- Aromatase (← links)
- Plakoglobin (← links)
- Long-chain-aldehyde dehydrogenase (← links)
- Glutathione synthetase (← links)
- MYH (← links)
- Public Health Genomics (← links)
- Preimplantation genetic diagnosis (← links)
- Shaking rat Kawasaki (← links)
- Glycogen storage disease type V (← links)
- Causes of hypoglycemia (← links)
- Rotor syndrome (← links)
- Lucey-Driscoll syndrome (← links)
- V-ATPase (← links)
- Perhexiline (← links)
- C syndrome (← links)
- Cytochrome C1 (← links)
- Fountain syndrome (← links)
- Hereditary inclusion body myopathy (← links)
- Hypophosphatasia (← links)
- Kugelberg-Welander disease (← links)
- Pacman dysplasia (← links)
- Spinal Muscular Atrophy Type 2 (← links)
- Zaspopathy (← links)
- Bernard-Soulier syndrome (← links)
- Hypochromic anemia (← links)
- Skin cancer (← links)
- Majewski's polydactyly syndrome (← links)
- Lung pinprick condition (← links)
- Seckel syndrome (← links)
- Selective immunoglobulin A deficiency (← links)
- Common variable immunodeficiency (← links)
- 2,8 dihydroxy-adenine urolithiasis (← links)
- 3m syndrome (← links)
- Zazam Sheriff Phillips syndrome (← links)
- Cutis laxa (← links)
- Uncombable hair syndrome (← links)
- Erythropoietic protoporphyria (← links)
- Freeman-Sheldon syndrome (← links)
- Glycogen storage disease (← links)
- Glycogen storage disease type VI (← links)
- Glycogen storage disease type VII (← links)
- Sly syndrome (← links)
- Hyper IgM syndrome (← links)
- Limb-girdle muscular dystrophy (← links)
- Synovitis (← links)
- Naxos disease (← links)
- Olivopontocerebellar atrophy (← links)
- Purine nucleoside phosphorylase deficiency (← links)
- Neuronal ceroid lipofuscinosis (← links)
- Arterial tortuosity syndrome (← links)
- Centronuclear myopathy (← links)
- Alpers' disease (← links)
- Leukoencephalopathy with vanishing white matter (← links)
- CAMFAK syndrome (← links)
- Werdnig-Hoffman disease (← links)
- Grey platelet syndrome (← links)
- Juvenile primary lateral sclerosis (← links)
- Renal dysplasia-limb defects syndrome (← links)
- Senior-Løken syndrome (← links)
- Periodic fever syndrome (← links)
- ICD-10 Chapter VI: Diseases of the nervous system (← links)
- Hypobetalipoproteinemia (← links)
- Uridine monophosphate synthetase (← links)
- HBB (← links)
- Glycogen storage disease type IV (← links)
- Combined immunodeficiency (← links)
- Dor Yeshorim (← links)
- Persistent müllerian duct syndrome (← links)
- Normocytic anemia (← links)
- Hurler-Scheie syndrome (← links)
- Hemophilia C (← links)
- Diaphragmatic hernia (← links)
- Beta-glucuronidase (← links)
- Dysbetalipoproteinemia (← links)
- Keutel syndrome (← links)
- Triosephosphate isomerase deficiency (← links)
- TMPRSS3 (← links)
- Woodhouse-Sakati syndrome (← links)
- ST3GAL5 (← links)
- CLN5 (← links)
- NNT (gene) (← links)
- ALOX12B (← links)
- WFS1 (← links)
- ELAC2 (← links)
- TACSTD2 (← links)
- Bietti's crystalline dystrophy (← links)
- EEM syndrome (← links)
- Parkinson’s disease (← links)
- Hypervalinemia (← links)
- Organic acidemia (← links)
- Carnosinemia (← links)
- Microvillous inclusion disease (← links)
- Cross syndrome (← links)
- VLDLR-associated cerebellar hypoplasia (← links)
- Winchester syndrome (← links)
- Normochromic anemia (← links)
- D-Glyceric acidemia (← links)