Pages that link to "Autosomal recessive"
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The following pages link to Autosomal recessive:
Displayed 500 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)
- Urocanic aciduria (← links)
- 2-Hydroxyglutaric aciduria (← links)
- L2HGDH (← links)
- RPGRIP1L (← links)
- Aicardi-Goutieres syndrome (← links)
- Neuromuscular junction disease (← links)
- Shwachman-Diamond syndrome (patient information) (← links)
- Macular degeneration (patient information) (← links)
- Pulmonic regurgitation pathophysiology (← links)
- Spinal muscular atrophy overview (← links)
- Spinal Muscular Atrophy Overview (← links)
- Spinal Muscular atrophy overview (← links)
- Spinal Muscular atrophy types (← links)
- Spinal Muscular atrophy Overview (← links)
- Spinal muscular atrophy types (← links)
- Tricuspid atresia overview (← links)
- Tricuspid atresia causes (← links)
- Basal cell carcinoma risk factors (← links)
- Pancytopenia (← links)
- Hereditary nonpolyposis colorectal cancer classification (← links)
- Hereditary nonpolyposis colorectal cancer differential diagnosis (← links)
- Myelodysplastic syndrome differential diagnosis (← links)
- Cystic fibrosis overview (← links)
- Cystic fibrosis pathophysiology (← links)
- Cystic fibrosis historical perspective (← links)
- Bonnemann-Meinecke-Reich syndrome (← links)
- Early myoclonic encephalopathy (← links)
- Pyridoxamine 5-prime-phosphate oxidase deficiency (← links)
- Tricho-hepato-enteric syndrome (← links)
- Mental retardation-epilepsy-bulbous nose (← links)
- Faisalabad histiocytosis (← links)
- Rosai Dorfman disease (← links)
- Desmosterolosis (← links)
- Chédiak-Higashi syndrome (patient information) (← links)
- Neutral lipid storage disease (← links)
- Wolcott-Rallison syndrome (← links)
- Galactose epimerase deficiency (← links)
- Stuve-Weidemann syndrome (← links)
- Polycystic kidney disease overview (← links)
- Urbach–Wiethe disease (← links)
- Polycystic kidney disease classification (← links)
- Sickle-cell disease overview (← links)
- Sickle-cell disease classification scheme (← links)
- Sickle-cell disease pathophysiology (← links)
- Arthrogryposis classification (← links)
- Arthrogryposis causes (← links)
- Gaucher's disease pathophysiology (← links)
- Ataxia telangiectasia differential diagnosis (← links)
- Porphyria pathophysiology (← links)
- Porphyria medical therapy (← links)
- Charcot-Marie-Tooth disease classification (← links)
- Wilson's disease overview (← links)
- Wilson's disease pathophysiology (← links)
- Atopic dermatitis differential diagnosis (← links)
- Dilated cardiomyopathy screening (← links)
- Long QT Syndrome overview (← links)
- Long QT Syndrome classification (← links)
- Long QT Syndrome pathophysiology (← links)
- Long QT Syndrome natural history, complications and prognosis (← links)
- Amyotrophic lateral sclerosis overview (← links)
- 22q11.2 deletion syndrome overview (← links)
- Albinism classification (← links)
- 22q11.2 deletion syndrome pathophysiology (← links)
- Albinism pathophysiology (← links)
- Amyotrophic lateral sclerosis laboratory findings (← links)
- Multiple sclerosis differential diagnosis (← links)
- Secondary adrenal insufficiency pathophysiology (← links)
- Thalassemia overview (← links)
- Thalassemia pathophysiology (← links)
- Iron deficiency anemia differential diagnosis (← links)
- Hemolytic anemia pathophysiology (← links)
- Hypopituitarism causes (← links)
- Sickle-cell disease causes (← links)
- Hemochromatosis echocardiography or ultrasound (← links)
- Alopecia pathophysiology (← links)
- Sickle-cell disease classification (← links)
- Arrhythmogenic right ventricular dysplasia overview (← links)
- Thrombocytopenia differential diagnosis (← links)
- Tremor pathophysiology (← links)
- Diabetes mellitus type 2 risk factors (← links)
- Androgen insensitivity syndrome differential diagnosis (← links)
- Whipple's disease differential diagnosis (← links)
- Familial adenomatous polyposis overview (← links)
- Familial adenomatous polyposis pathophysiology (← links)
- Hypogonadism pathophysiology (← links)
- Pseudohypoparathyroidism pathophysiology (← links)
- 17-beta-hydroxysteroid dehydrogenase deficiency overview (← links)
- 17-beta-hydroxysteroid dehydrogenase deficiency molecular genetic studies (← links)
- 21-Hydroxylase Deficiency causes (← links)
- 21-Hydroxylase Deficiency screening (← links)
- Growth hormone deficiency classification (← links)
- 21-Hydroxylase Deficiency molecular genetic studies (← links)
- 5-alpha-reductase deficiency overview (← links)
- Laron syndrome overview (← links)
- Laron syndrome pathophysiology (← links)
- Autoimmune polyendocrine syndrome overview (← links)
- Lipoid congenital adrenal hyperplasia overview (← links)
- Autoimmune polyendocrine syndrome pathophysiology (← links)
- Autoimmune polyendocrine syndrome differential diagnosis (← links)
- Glycogen storage disease type I overview (← links)
- Autoimmune polyendocrine syndrome primary prevention (← links)
- Glycogen storage disease type I pathophysiology (← links)
- Glycogen storage disease type I causes (← links)
- Glycogen storage disease type II overview (← links)
- Glycogen storage disease type II pathophysiology (← links)
- Glycogen storage disease type II causes (← links)
- 21-hydroxylase deficiency overview (← links)
- 21-hydroxylase deficiency pathophysiology (← links)
- 21-hydroxylase deficiency epidemiology and demographics (← links)
- Hypoaldosteronism pathophysiology (← links)
- Congenital hyperinsulinism classification (← links)
- Nephrogenic diabetes insipidus overview (← links)
- Hypoparathyroidism pathophysiology (← links)
- Hypoparathyroidism causes (← links)
- Nephrogenic diabetes insipidus secondary prevention (← links)
- Diamond-Blackfan anemia causes (← links)
- Diamond-Blackfan anemia differential diagnosis (← links)
- Hemophagocytic lymphohistiocytosis classification (← links)
- Aplastic anemia differential diagnosis (← links)
- Hemophagocytic lymphohistiocytosis causes (← links)
- Macrocytic anemia differential diagnosis (← links)
- Fanconi anemia overview (← links)
- Anemia of chronic disease differential diagnosis (← links)
- Fanconi anemia causes (← links)
- Autoimmune hemolytic anemia differential diagnosis (← links)
- Hereditary elliptocytosis overview (← links)
- Hereditary elliptocytosis epidemiology and demographics (← links)
- Hereditary elliptocytosis pathophysiology (← links)
- Neonatal jaundice pathophysiology (← links)
- Folate deficiency differential diagnosis (← links)
- Sideroblastic anemia overview (← links)
- Sideroblastic anemia causes (← links)
- Hereditary spherocytosis overview (← links)
- Sideroblastic anemia classification (← links)
- Sideroblastic anemia differential diagnosis (← links)
- Hereditary spherocytosis epidemiology and demographics (← links)
- Hereditary spherocytosis classification (← links)
- Hereditary spherocytosis causes (← links)
- Hereditary spherocytosis screening (← links)
- X-linked agammaglobulinemia differential diagnosis (← links)
- Paroxysmal nocturnal hemoglobinuria differential diagnosis (← links)
- Anemia of prematurity differential diagnosis (← links)
- Von Willebrand disease overview (← links)
- Von Willebrand disease pathophysiology (← links)
- Primary ciliary dyskinesia overview (← links)
- Primary ciliary dyskinesia pathophysiology (← links)
- Hemothorax pathophysiology (← links)
- Polycystic kidney disease differentiating polycystic kidney disease from other diseases (← links)
- Medullary sponge kidney differential diagnosis (← links)
- Potter syndrome classification (← links)
- Potter syndrome pathophysiology (← links)
- Bartter syndrome differential diagnosis (← links)
- Abderhalden-Kaufmann-Lignac syndrome overview (← links)
- LQT1 (← links)
- Long QT Syndrome genetic studies (← links)
- Braddock syndrome (← links)
- Pierson syndrome (← links)
- Braun-Bayer syndrome (← links)
- Grange syndrome (← links)
- Congenital generalized lipodystrophy (← links)
- Salih myopathy (← links)
- Retinitis causes (← links)
- Retinitis risk factors (← links)
- Caroli's disease causes (← links)
- Familial mediterranean fever overview (← links)
- Familial mediterranean fever pathophysiology (← links)
- Familial mediterranean fever differential diagnosis (← links)
- Lactose intolerance overview (← links)
- Lactose intolerance pathophysiology (← links)
- Alstrom syndrome (patient information) (← links)
- Alstrom syndrome differential diagnosis (← links)
- Alstrom syndrome primary prevention (← links)
- Lactose intolerance classification (← links)
- Blepharitis causes (← links)
- Hyperhidrosis overview (← links)
- WBR0052 (← links)
- Hennekam syndrome (← links)
- WBR0098 (← links)
- Idiopathic infantile arterial calcification (← links)
- Carvajal-Huerta syndrome (← links)
- Idiopathic infantile arterial calcification overview (← links)
- WBR0103 (← links)
- Pseudoxanthoma elasticum overview (← links)
- Pseudoxanthoma elasticum classification (← links)
- WBR0191 (← links)
- Primary hypertriglyceridemia (← links)
- WBR0422 (← links)
- Niemann-Pick disease overview (← links)
- WBR0787 (← links)
- Fryns syndrome (← links)
- WBR0321 (← links)
- Galactosemia classification (← links)
- WBR0981 (← links)
- WBR0982 (← links)
- WBR0987 (← links)
- WBR0989 (← links)
- Ehlers–Danlos syndrome (← links)
- WBR0117 (← links)
- Congenital disorders of the bone marrow (← links)
- Velaglucerase alfa (← links)
- Dyslipidemia resident survival guide (← links)
- Phenylketonuria overview (← links)
- Phenylketonuria pathophysiology (← links)
- Young–Simpson syndrome (← links)
- Hemoglobin Lepore syndrome (← links)
- Wrinkly skin syndrome (← links)
- Mungan syndrome (← links)
- Distal spinal muscular atrophy type 1 (← links)
- Pontocerebellar hypoplasia (← links)
- Microvillus inclusion disease (← links)
- 11β-hydroxylase deficiency pathophysiology (← links)
- Sandbox cah 17 (← links)
- 17 alpha-hydroxylase deficiency pathophysiology (← links)
- 17 alpha-hydroxylase deficiency differential diagnosis (← links)
- 17 alpha-hydroxylase deficiency overview (← links)
- Hartnup Disease causes (← links)
- IgG deficiency (← links)
- Glanzmann's thrombasthenia classification (← links)
- Glanzmann's thrombasthenia pathophysiology (← links)
- Glanzmann's thrombasthenia overview (← links)
- Differentiating celiac disease from other diseases (← links)
- Differentiating Osteoporosis from other diseases (← links)
- Differentiating Albinism from other diseases (← links)
- Glycogen storage disease type I screening (← links)
- CANDLE syndrome (← links)
- Subarachnoid hemorrhage screening (← links)
- Pulmonic regurgitation screening (← links)
- Sebelipase alfa (← links)
- Chronic diarrhea differential diagnosis (← links)
- Primary amenorrhea DDx (← links)
- Hereditary pancreatitis overview (← links)
- Hereditary pancreatitis classification (← links)
- Hereditary pancreatitis pathophysiology (← links)
- Chronic diarrhea malabsorption DDx (← links)
- Sandbox: malabsorption (← links)
- Glycogen storage disease type III overview (← links)
- Glycogen storage disease type III pathophysiology (← links)
- Glycogen storage disease type III causes (← links)
- Glycogen storage disease type III screening (← links)
- Myocilin (← links)
- Roundabout (gene family) (← links)
- GABAA-rho receptor (← links)
- TENM3 (← links)
- CLPB (← links)
- PAM16 (← links)
- ENO3 (← links)
- ALOXE3 (← links)
- SLC13A5 (← links)
- SEC23B (← links)
- GM2A (← links)