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Company Thomson / HP / / IndustryTerm human disease network / / MedicalCondition Melnick-Needles hereditary dermopathy / microcephaly / congenital muscular dystrophy Unna-Thost disease / Holoprosencephaly Medulloblastoma Hyperostosis / HIV / dysarthria / cavernous malformations Ovarian hyperstimulation syndrome Placental steroid sulfatase deficiency / endosteal Hypodontia Marfan Aortic syndrome aneurysm PTCH Norrie disease / hyperparathyroidism / Desmoid Ataxia-telangiectasia lung_cancer Cafe-au-lait Schizophrenia NLGN3 MECP2 syndrome disease / hypercalcemia deficiency / Adrenocortical Ceroid-lipofuscinosis Smith-Fineman-Myers Amelogenesis myopathy syndrome Chorea / Fanconi Estrogen SLC6A4 AXIN2 Neurofibromatosis NF1 Neurofibromatosis disorder / PRNP CTLA4 blood_type RAG1 Hyperparathyroidism Goiter CACNA1A Rh-mod G6PD GSS Thyroid syndrome Creutzfeldt-Jakob TPO PDGFRA RAG2 hormone SDHB Insomnia Omenn SDHD PGK1 disease Graves Myelofibrosis / SERPINA3 Sickle Pancreatitis TF Hand-foot-uterus hypertension / McCune-Albright syndrome / Shields type Dermatofibrosarcoma / Progressive external ophthalmoplegia / dsytrophy Rabson-Mendenhall syndrome / SFTPC hyperlipemia right ventricle Synostoses syndrome Congestive Aromatase disease PEX7 PSAP syndrome / adult Wolfram Calcinosis / cortical dysplasia / sensorineural Hemosiderosis / EVC hypogonadism HARP / Hypoaldosteronism GP1BB FUT2 Situs disease Bosley-Salih-Alorainy Ovarioleukodystrophy MASA Leiomyomatosis Agammaglobulinemia syndrome Pseudohermaphroditism / muscular dystrophy PRKAG2 Wolff-Parkinson-White syndrome TAZ Barth syndrome / primary spontaneous Prion disease / disorder / PITX2 Ring_dermoid / tumor anemia DCLRE1C / fibroblastoma Cancer defect/deficiency / adult forms Schwartz-Jampel syndrome / syndrome Hearing loss / Muir-Torre PTPN22 cancer / Placental Autism SOX3 Hypertension Wiskott-Aldrich / aceruloplasminemia High-molecular-weight kininogen deficiency Homocystinuria-megaloblastic anemia / CPT deficiency / Hypereosinophilic Hypocalciuric Paragangliomas Adenosine_deaminase Combined Cerebellar syndrome / Myotonia / syndrome Birt-Hogg-Dube WT1 NBN Waardenburg-Shah disease Schwannomatosis Adrenal_cortical syndrome / hypopigmentation syndrome Chronic infections / muscular dystrophy Fatty liver / Xeroderma NR0B1 Exostoses / familial Cold-induced autoinflammatory syndrome Colonic aganglionosis / autosomal recessive Methylcobalamin deficiency / hypothyroidism / microcytic Spina disease / paravenous chorioretinal atrophy Pituitary ACTH-secreting adenoma Pneumonitis / ataxia thyroid CASR disease Hemiplegic_migraine / Basal adenoma CYP11B2 overload/deficiency lipofuscinosis SPINK1 syndrome disease / NSD1 syndrome Cystinuria Dent Dysprothrombinemia familial_benign anemia Erythrocytosis / Diabetes / syndrome Brugada syndrome Cramps / ataxia Merkel_cell Hypocalcemia Carcinoidcarcinoma tumors / autosomal recessive Sandhoff disease / right ventricular dysplasia Athabaskan brainstem dysgenesis syndrome Attention-deficit hyperactivity disorder Bannayan-Riley / retina Central hypoventilation syndrome Cerebrooculofacioskeletal syndrome Cerebrovascular disease / osteopoikilosis Methionine adenosyltransferase deficiency / dysplasia Cyclic ichthyosis / Dilated cardiomyopathy / Neurofibromatosis-Noonan syndrome Nevus / complex deficiency Myelomonocytic leukemia / Pancreatic ENPP1 disease / deficiency Alpha-thalassemia/mental retardation syndrome Alternating hemiplegia / tubular SLC2A2 Alzheimer FGG Myelogenous ARX dysgenesis CASP10 Autoimmune Androgen Thrombophilia / Tuberculosis Adrenoleukodystrophy PANK2 / maxillary central incisor Spondylocarpotarsal synostosis syndrome Stapes ankylosis syndrome / desquamative interstitial Pneumothorax / OPN1MW Rapp-Hodgkin syndrome / Lange-Nielsen syndrome Juvenile polyposis/hereditary / LCHAD LPL disease Combined CLCN5 disease failure HFE syndrome LIG4 NOG Pulmonary PAH / Mucopolysaccharidosis Hoyeraal-Hreidarsson / acrodental myopathy Chudley-Lowry Sarcoidosis / disorders / dizygotic papular lesions COL10A1 RMRP disease / cystic kidney disease Melorheostosis / lipase Laron Alport syndrome / endothelial corneal dystrophy Giant platelet disorder / infantile Hyperandrogenism Aldosteronism Chondrocalcinosis / hyperinsulinemic hypoglycemia / Hyperalphalipoproteinemia HarderoporphyrinuriaHyper-IgD GLB1 Salla syndrome / respiratory failure Thanatophoric dysplasia / Isolated disorders / mitochondrial DNA deletions Prolactinoma / idiopathic Gerstmann-Straussler Favism deficiency / left ventricular myocardium Norwalk virus infection / CTSC Mephenytoin spoldylitis ANKH Trichothiodystrophy Paget anemia / Microphthalmia albinism Conjunctivitis / Plasminogen Methemoglobinemia syndrome / MC1R Fitzgerald factor disease anemia type syndrome / Spinocereballar Huntington Elliptocytosis Hemangioblastoma / COL1A2 OPA1 Glaucoma RASA1 Basal_cell carcinoma LRP5 Osteoporosis / congenita Shprintzen-Goldberg syndrome Peters Keratitis Eye anomaly Ectopia anomalies Coloboma / epidermolytic hyperkeratosis Dentinogenesis imperfecta / LCAT DRD5 fibrosis / Obsessive-compulsive / stromal RHAG Angiofibroma / periodic Thyrotoxic paralysis periodic paralysis Aniridia / Insulin resistance Squamous_cell Non-Hodgkin carcinoma / Hyperthyroidism / JAK2 Pheochromocytoma / SPTA1 syndrome anemia / white matter Lower motor neuron disease / angiopathy syndrome / Episodic G6PD Autoimmune disease IL2RG / Blepharophimosis / dyskinesia dysplasia Erythremias Acromesomelic Grebe SLC45A2 HLA-B deficiency STAT1 / sensitivity MKKS SHOX CYP19A1 Fibromatosisl Hematuria / Mast_cell RHCE of_lung SPTB MEN1 leukemia adenoma / syndrome Germ_cell toxicity Shah-Waardenburg Nasopharyngeal syndrome / PGK deficiency Myokymia / serous carcinoma / retinal syndromedystrophy Hemolytic-uremic syndrome / Enlarged syndrome / symphalangism Stevens-Johnson syndrome / NOS3 Saethre-Chotzen spasms / Myoglobinuria / Nevo syndrome COL3A1 Aneurysm / CF Tarsal-carpal coalition syndrome Tauopathy / deafness Keratosis / distress Chylomicronemia syndrome / MTR HBA2 Ovarian syndrome Leri-Weill Virilization poisoning CPOX SLC3A1 CYP21A2 MTRR Spondylometaphyseal Cartilage-hair ANTXR2 MVK syndrome rate Nemaline Osteolysis / ataxia Uterine Insensitivity Gastrointestinal adenoma / Hystrix-like ichthyosis / Osteopoikilosis nail TNFRSF11A Hyperprothrombinemia Tolbutamide Steatocystoma sensitivity systemic sclerosis Coproporphyria Mevalonicaciduria syndrome / imperfecta Coats disease Osteopetrosis NDP / chondrodysplasia punctata Robinow syndrome / hypertension / disease / fibrosis deficiency syndrome / cutaneous capillary-venous malformations Hypoparathyroidism-retardation-dysmorphism syndrome Hypoplastic enamel / SARS / mineral density variability Carpal tunnel syndrome / Cowden carcinoma Atopy disease Mesangial disease EDNRB Nijmegen_breakage Malaria NF2 Parkinson Histiocytoma CIITA / neonatal epilepsy Nephrogenic syndrome / leiomyoma to_pain / Preeclampsia NLGN4X Asperger Proud Adenoma / disease H._pylori infection BCG infection IFNGR1 Adrenomyeloneuropathy Synpolydactyly ABCD1 / mental retardation Total iodide organification defect Ventricular fibrillation / Unclassified Sea-blue_histiocyte disease Amyloidosis / Bare_lymphocyte Stomach syndrome PCWH Rhabdomyosarcoma syndrome WAGR cancer TGFBR2 / Adrenal disease Hypothyroidism / Creatine deficiency syndrome / adrenocortical disease / neoplasia complex Fraumeni Dyserythropoietic VHL syndrome TSHR Retinoblastoma Myxoma / cutaneous and uterine leiomyomata Optic nerve coloboma / inappropriate antidiuresis Neural tube defects / Glomerulocystic kidney disease / B lipodystrophy Mastocytosis / Systemic_lupus CDH1 Jackson-Weiss syndrome / FSHR dysplasia PXMP3 Resting gout metabolizer Lowe Hypoprothrombinemia syndrome HR Sialidosis / Abacavir Opremazole syndrome disease malformation syndrome / human disease / syndrome / genes connecting disorders / / OperatingSystem Leopard / / Organization ELN / VATER association / / Person Shah-Waardenburg Nasopharyngeal / Scott Liddle / Gilbert Palmoplantar / Salih-Alorainy Ovarioleukodystrophy / Denys-Drash Wilms Mesothelioma / Kenny-Caffey Campomelic / Heinz Hypolactasia / / Position dysplasia MATN3 Marshall / Coumarin resistance Infantile_spasm syndrome CYP2A6 Nicotine addiction CHRNA4 Usher / / Product Vitamin K / ACTH / Tolbutamide / Nicotine / carbamazepine / Abacavir / Fluorouracil / Adenosine / Beta-2 / / ProvinceOrState Newfoundland / / Technology Alpha / EBD / ATM / condensation / DSP / /
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The human disease network ′ A-LProc Natl Acad Sci USA 104:Goh K-I, Cusick ME, Valle D, Childs B, Vidal M, Barabasi Urolithiasise Caffey