Pages that link to "Mendelian Inheritance in Man"
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The following pages link to Mendelian Inheritance in Man:
Displayed 26 items.
- ASPM (Genetics) (← links)
- HomoloGene (← links)
- Mendelian inheritance (← links)
- Entrez (← links)
- BLAST (← links)
- Bioinformatic Harvester (← links)
- SOSUI (← links)
- GFP-cDNA (← links)
- Information Hyperlinked over Proteins (← links)
- Netrin (← links)
- Transglutaminase (← links)
- UniProt (← links)
- GoPubMed (← links)
- Medical classification (← links)
- Diagnosis codes (← links)
- Ahmad Teebi (← links)
- Transglutamination (← links)
- Online Mendelian Inheritance in Man (redirect page) (← links)
- Pachydermoperiostosis (← links)
- Hypouricemia (← links)
- Cystinosis (← links)
- Hemopexin (← links)
- HLA-B27 (← links)
- Myoglobin (← links)
- Thiamine (← links)
- Follicle-stimulating hormone (← links)
- Congenital Absence of the Vas Deferens (← links)
- Von Hippel-Lindau disease (← links)
- 5q- syndrome (← links)
- Ectrodactyly (← links)
- Krause-Kivlin syndrome (← links)
- Larsen syndrome (← links)
- Oguchi disease (← links)
- Wallis Zieff Goldblatt syndrome (← links)
- Kindler syndrome (← links)
- Howel-Evans syndrome (← links)
- AREDYLD (← links)
- Young's syndrome (← links)
- Activated protein C resistance (← links)
- Adams Nance syndrome (← links)
- Adenylosuccinate lyase deficiency (← links)
- Aniridia (← links)
- Ataxia telangiectasia (← links)
- Ayazi syndrome (← links)
- Leber's congenital amaurosis (← links)
- Retinitis pigmentosa (← links)
- Bare lymphocyte syndrome (← links)
- Blue diaper syndrome (← links)
- DAB1 (← links)
- Tachykinin peptides (← links)
- Brain-derived neurotrophic factor (← links)
- Ribosomal s6 kinase (← links)
- TCF7L2 (← links)
- Fas ligand (← links)
- Lamin B receptor (← links)
- VLDL receptor (← links)
- RET proto-oncogene (← links)
- MEF2A (← links)
- Autosomal dominant hypophosphatemic rickets (← links)
- Amyloid beta (← links)
- Apolipoprotein E (← links)
- Tylosis (← links)
- Iron overload disorder (← links)
- Hereditary hemorrhagic telangiectasia (← links)
- Phenylthiocarbamide (← links)
- Krüppel (← links)
- Cleft chin (← links)
- Blood type (← links)
- Kell antigen system (← links)
- Kidd antigen system (← links)
- Colton antigen system (← links)
- Yt antigen system (← links)
- Plasmin (← links)
- Tissue factor pathway inhibitor (← links)
- Tissue factor (← links)
- African iron overload (← links)
- McLeod syndrome (← links)
- HLA-B (← links)
- Cenani Lenz syndactylism (← links)
- Congenital afibrinogenemia (← links)
- 2-Hydroxyglutaricaciduria (← links)
- 3 hydroxyisobutyric aciduria (← links)
- 3 methylcrotonic aciduria (← links)
- 6-Pyruvoyltetrahydropterin synthase deficiency (← links)
- Carpenter syndrome (← links)
- Citrullinemia (← links)
- Cockayne syndrome (← links)
- Crouzonodermoskeletal syndrome (← links)
- Dihydropyrimidine dehydrogenase deficiency (← links)
- GAPO syndrome (← links)
- Maple syrup urine disease (← links)
- Mucopolysaccharidosis (← links)
- Ornithine translocase deficiency (← links)
- Periodic paralysis (← links)
- Philadelphia chromosome (← links)
- Photic sneeze reflex (← links)
- Recessive multiple epiphyseal dysplasia (← links)
- SADDAN (← links)
- Sarcosinemia (← links)
- Turcot syndrome (← links)
- Variegate porphyria (← links)
- WAGR syndrome (← links)
- Weissenbacher-Zweymüller syndrome (← links)
- X-linked ichthyosis (← links)
- ZAP70 deficiency (← links)
- Epigenetics (← links)
- PGL2 (← links)
- Abl gene (← links)
- Microcephalin (← links)
- COL1A1 (← links)
- CFTR (gene) (← links)
- HD (gene) (← links)
- MUTYH (← links)
- TBX1 (← links)
- PPOX (← links)
- IKBKAP (← links)
- Pax genes (← links)
- 3-hydroxy-3-methylglutaryl-CoA lyase (← links)
- LMNA (← links)
- UDP galactose epimerase (← links)
- Titin (← links)
- Ataxin 7 (← links)
- Thrombopoietin (← links)
- Superoxide dismutase (← links)
- Huntingtin (← links)
- Electron-transferring-flavoprotein dehydrogenase (← links)
- SLC26A2 (← links)
- Myelin oligodendrocyte glycoprotein (← links)
- COL11A2 (← links)
- VPS13B (← links)
- ADAMTS13 (← links)
- Abelson leukemia virus protein (← links)
- Fukutin (← links)
- Mannan-binding lectin (← links)
- Lactate dehydrogenase (← links)
- Mevalonate kinase (← links)
- N-acetylglucosamine-1-phosphate transferase (← links)
- ETV6 (← links)
- Fumarylacetoacetate hydrolase (← links)
- Glial fibrillary acidic protein (← links)
- Wiskott-Aldrich syndrome protein (← links)
- OCRL (← links)
- Monoamine oxidase A (← links)
- Acetylserotonin O-methyltransferase (← links)
- Doublecortin (← links)
- National Center for Biotechnology Information (← links)
- Fatal familial insomnia (← links)
- Hyper IgM Syndrome Type 5 (← links)
- Wikipedia:WikiProject Molecular and Cellular Biology/Style guidelines (← links)
- Lucey-Driscoll syndrome (← links)
- Hyperpipecolatemia (← links)
- Pyruvate kinase (← links)
- Fissured tongue (← links)
- Phosphate-regulating endopeptidase gene (← links)
- Nodal (protein) (← links)
- Troponin C (← links)
- TRPV4 (← links)
- BACE2 (← links)
- Tuftsin (← links)
- Hydrogen cyanide (← links)
- Cyanide (← links)
- Xanthine oxidase (← links)
- Bone morphogenetic protein 4 (← links)
- Rab (G-protein) (← links)
- Cytochrome C1 (← links)
- Adiposis dolorosa (← links)
- Adrenocorticotropic hormone deficiency (← links)
- Cystic medial necrosis (← links)
- Familial male precocious puberty (← links)
- Fountain syndrome (← links)
- Glucocorticoid deficiency 1 (← links)
- Hypertrichosis lanuginosa (← links)
- Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency (← links)
- Methylmalonic acidemia (← links)
- Pacman dysplasia (← links)
- Zaspopathy (← links)
- Hereditary spherocytosis (← links)
- Congenital absence of the vas deferens (← links)
- Zori Stalker Williams syndrome (← links)
- Freeman-Sheldon syndrome (← links)
- Hyperammonemia (← links)
- Spermatogenesis arrest (← links)
- ICF syndrome (← links)
- Meleda Disease (← links)
- Michelin tire baby syndrome (← links)
- Mullerian agenesis (← links)
- Pachygyria (← links)
- Pentalogy of Cantrell (← links)
- Progressive supranuclear palsy (← links)
- Mevalonic aciduria (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- Neuronal ceroid lipofuscinosis (← links)
- HEC syndrome (← links)
- Biomolecular Object Network Databank (← links)
- Donohue syndrome (← links)
- Monosomy 9p (← links)
- Nezelof syndrome (← links)
- Grey platelet syndrome (← links)
- Patterson syndrome (← links)
- Da Costa's syndrome (← links)
- Hyper IgM Syndrome Type 2 (← links)
- Regulatory T cell (← links)
- Melanocortin 1 receptor (← links)
- CD244 (← links)
- Phosphoinositide 3-kinase (← links)
- C-Raf (← links)
- Neuregulin (← links)
- Hedgehog signaling pathway (← links)
- H19 (gene) (← links)
- Branchio-oto-renal syndrome (← links)
- PACS1 (← links)
- CCNB1IP1 (← links)
- TFAP2A (← links)
- RIPK1 (← links)
- Sequestosome 1 (← links)
- Interferon gamma receptor 1 (← links)
- NT5E (← links)
- SAT1 (gene) (← links)
- KCNJ5 (← links)
- SLC25A3 (← links)
- Thiamin (← links)
- Antley-Bixler syndrome (← links)
- MEF2C (← links)
- Rothmund-Thomson syndrome (← links)
- SLC25A10 (← links)
- Brunner syndrome (← links)
- Potassium cyanide (← links)
- Cytochrome b5 (← links)
- Freckles (← links)
- Carnosinemia (← links)
- Microvillous inclusion disease (← links)
- Phene (← links)
- Jansky-Bielschowsky disease (← links)
- CD79A (← links)
- Gunther disease (← links)
- Argininemia (← links)
- Acrocephalosyndactylia (← links)
- Hyper-IgM syndrome type 2 (← links)
- Hyper-IgM syndrome type 5 (← links)
- Beta amyloid (← links)
- LAMP2 (← links)
- Timeline of tuberous sclerosis (← links)
- Beta-mannosidosis (← links)
- Fibrochondrogenesis (← links)
- Hexokinase deficiency (← links)
- HK1 (← links)
- Acrocallosal syndrome (← links)
- Ichthyosis bullosa of Siemens (← links)
- Color blindness (patient information) (← links)
- Hypoplastic left heart syndrome causes (← links)
- Hereditary nonpolyposis colorectal cancer pathophysiology (← links)
- Geroderma osteodysplastica (← links)
- Hyperglycerolemia (← links)
- Aplasia cutis congenita (← links)
- Lawrence-Moon syndrome (← links)
- Achalasia-addisonian syndrome (← links)
- Galactose epimerase deficiency (← links)
- Arthrogryposis classification (← links)
- Gaucher's disease pathophysiology (← links)
- Ataxia telangiectasia pathophysiology (← links)
- Amenorrhea pathophysiology (← links)
- Thalassemia pathophysiology (← links)
- Maturity onset diabetes of the young pathophysiology (← links)
- Delayed puberty pathophysiology (← links)
- Nephrogenic diabetes insipidus causes (← links)
- Papillorenal syndrome overview (← links)
- Potter syndrome classification (← links)
- Retinitis causes (← links)
- Dyskeratosis congenita overview (← links)
- Buschke–Ollendorff syndrome (← links)
- Schindler disease (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Hypertryptophanemia (← links)
- WARG syndrome (← links)
- Basement membrane corneal dystrophy (← links)
- Pontocerebellar hypoplasia (← links)
- Permanent neonatal diabetes mellitus (← links)
- Microvillus inclusion disease (← links)
- Transthyretin-related hereditary amyloidosis (← links)
- Sandbox: HTM (← links)
- Lethal congenital contracture syndrome (← links)
- Hartnup Disease overview (← links)
- Hartnup Disease causes (← links)
- Hartnup Disease pathophysiology (← links)
- Propionic acidemia overview (← links)
- Propionic acidemia pathophysiology (← links)
- Propionic acidemia epidemiology and demographics (← links)
- Johanson-Blizzard syndrome (← links)
- KIRREL (← links)
- GON4L (← links)
- EPHA10 (← links)
- UDP glucuronosyltransferase 1 family, polypeptide A1 (← links)
- Ectodysplasin A receptor (← links)
- Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A (← links)
- Roundabout (gene family) (← links)
- Collagen, type VII, alpha 1 (← links)
- ATG7 (← links)
- Slit (protein) (← links)
- ETFDH (← links)
- Kinesin family member 11 (← links)
- Solute carrier family 25 member 22 (← links)
- SYT1 (← links)
- Enolase 2 (← links)
- SLC17A8 (← links)
- GJB6 (← links)
- C14orf104 (← links)
- TGM5 (← links)
- Fibrillin 1 (← links)
- UQCRC2 (← links)
- COQ9 (← links)
- Collagen, type I, alpha 1 (← links)
- COX10 (← links)
- KLF1 (← links)
- Tubulin beta-4A chain (← links)
- Beta-secretase 2 (← links)
- Collagen, type XI, alpha 2 (← links)
- PDSS2 (← links)
- KLF14 (← links)
- ABL (gene) (← links)
- PHF8 (← links)
- TBX22 (← links)
- Tsix (← links)
- Wiskott–Aldrich syndrome protein (← links)
- GJB1 (← links)
- Cytochrome c oxidase subunit I (← links)
- DNAAF2 (← links)
- PET117 (← links)
- TMEM8B (← links)
- TMEM70 (← links)
- Twinkle (protein) (← links)
- Roundabout family (← links)
- PET100 (← links)
- COA6 (← links)
- SLC25A46 (← links)
- Sandbox:kalpana (← links)
- Template:OMIM (← links)
- Template:OMIM/doc (← links)
- Template:OMIM6 (← links)
- Zebrafish (← links)
- Mitocheck (← links)
- Sciencenet (← links)
- Flybase (← links)
- Template:OMIM3 (← links)
- Template:OMIM4 (← links)
- Template:OMIM5 (← links)
- Template:Harvesternavi (← links)