The Human Disease Network - Barabasi Lab
Alopecia universalis Alpers syndrome 87 Alpha-actinin-3 deficiency 92 Alport syndrome hereditary benign 320 Chudley-Lowry syndrome 329 Chylomicron retention disease Ciliary dyskinesia Hemochromatosis Hemoglobi_H disease Hemophilia Heterotaxy Heterotopia Hex_A ... Fetch Content
ID Panel Indikationen 120614 - MedUni Wien: Startseite
O Alopecia Universalis Congenita (ALUNC) HR O Darier Disease ATP2A2 O Dyskeratosis Congenita DKC1 O Epidermolysis O HFE-Associated Hereditary Hemochromatosis HFE O Hunter Syndrome (MPSII) IDS O Hurler Syndrome (MPSI) IDUA O ... Retrieve Doc
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Hereditary disorder of the urinary system (disorder) 36388008 Stricture of pelviureteric junction Stricture of pelviureteric junction (disorder) 36775008 Displaced ureteric orifice Ectopic insertion of ureter Anomalous implantation of ureteric orifice ... Fetch Here
Reproductive Genetics Institute (RGI)
Alopecia universalis congenita; alunc hr hemochromatosis; hfe hfe hemoglobin--alpha locus 1; hba1 hba1 hereditary sensory and autonomic, type i; hsan1 sptlc1 neuropathy, hereditary sensory and autonomic, type iii; hsan3 ikbkap ... Access Doc
20 Alopecia universalis; 21 Artralgia; 22 Colangite; 23 Cardiopatia congênita; HFE hereditary hemochromatosis) {{Info/Patologia | Nome = Hemochromatosis type 1 | Imagem = | Legenda = | CID10 = {{CID10|E|83|1|e|70}} | CID9 ... Read Article
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Hereditary neuropathy with liability to pressure palsies D00015 Glutamine D08133 Alopecia universalis H00780 Atrichia with papular lesions Cluster 243 H00129 Hunter syndrome Juvenile hemochromatosis H01196 Hypochromic microcytic anemia H00067 Friedreich ataxia Cluster 287 ... Content Retrieval
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Www.nature.com
Hereditary, 229050 (3) SLC5A5,NIS,TDH1 Hemochromatosis, 235200 (3); {Microvascular complications of diabetes7}, 612635 (3); {Porphyria variegata, Alopecia universalis, 203655 (3); Atrichia with papular lesions,209500 (3); ... Visit Document
Ion AmpliSeq™ Inherited Disease Panel Target Gene List
Ion AmpliSeq ™ Inherited Disease Panel target gene list Symbol Disease ENG Hereditary Hemorrhagic Telangiectasia EXT1 Exostoses, Multiple, HR Alopecia Universalis Congenita (ALUNC) IDS Hunter Syndrome (MPSII) IDUA Hurler Syndrome ... Document Viewer
Alopecia universalis congenita; alunc 全身性脱毛症 hr hemochromatosis; hfe ヘモクロマト－シス hfe hemoglobin—alpha locus 1; hba1 ヘモグロビン アルファー1 hba1 . neuropathy, hereditary sensory ... Return Doc
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Corneal dystrophy, hereditary polymorphous posterior, 2, 122000 (3) 1p34.3-p32.1 MUTYH MutY, E. coli, homolog of Adenomas, multiple colorectal, 608456 (3) Hemochromatosis, type 4, 606069 (3) Alopecia universalis, 203655 (3); Atrichia with papular lesions, 209500 (3) 8p21.1 ... View Doc
Auftrag Zur DNA Diagnostik - MedUni Wien: Startseite
O Alopecia Universalis Congenita (ALUNC) HR O O HFE-Associated Hereditary Hemochromatosis HFE O Hunter Syndrome (MPSII) IDS O Hurler Syndrome (MPSI) IDUA O Hydroxymethylbilane Synthase (HMBS) Deficiency HMBS O Hypophosphatasia ... Retrieve Full Source
PNAS - University Of Notre Dame
Alopecia universalis Alpers syndrome 87 Alpha-actinin-3 deficiency 92 Alport syndrome hereditary benign 320 Chudley-Lowry syndrome Chylomicron retention disease Ciliary dyskinesia Hemochromatosis Hemoglobi_H disease Hemophilia Heterotaxy Heterotopia Hex_A ... View Document
Book C, Supplement No. 30 - Veterans Benefits Administration Home
Schedule for Rating Disabilities. Veterans Benefits Administration. Alopecia: Areata 7831 4.118. Scarring 7830 4.118. Hemochromatosis 7345 4.114. Hemorrhoids, external or internal 7336 4.114. Hepatitis (B & C) 7345, 7354 4.114. ... Doc Retrieval
Vitiligo - Wikipedia, The Free Encyclopedia
Vitiligo where little pigmented skin remains is referred to as vitiligo universalis. pernicious anemia, alopecia areata, and systemic lupus erythematosus. Among the inflammatory products of NALP1 are caspase 1 Hemochromatosis; Iron metallic discoloration; Pigmented purpuric ... Read Article
Www.joshcorwin.com
( pigmentation - Hypermelanosis, Addison’s disease, Hemochromatosis, Acanthosis nigricans. Red - Inflammation, Port-Wine stain, Hemangioma. Blue - Cyanosis, Mongolian spot. hereditary epithelial tumor. Usually asymptomatic. Alopecia universalis - complete loss of all body hair. ... Get Doc
Hair 2000, Derm Facts
Alopecia universalis loss of all body hair; alopecia areata, exfoliative (Hallopeau-Siemens), folliculitis decalvans, Graham-Little s., Gunther’s d., hemochromatosis, ichthyosis (congenital erythrodermic pseudo pili annulati non-hereditary, no hair shaft cortex ... View This Document
Table Of Contents Part I: The Physiology Of The Pigmentary ...
Hereditary Sclerosing Poikiloderma Alopecia Areata (Wiete Westerhof). Heterochromia Irides (Wiete Westerhof, David Njoo, & Henk E. Menke ). Dyschromatosis Universalis Hereditaria (Eulalia Baselga & Nancy Burton Esterly ). ... Retrieve Document
Ichthyosis - Wikipedia, The Free Encyclopedia
Ichthyosis follicularis with alopecia and photophobia syndrome: MBTPS2: Membrane-bound transcription factor peptidase, site 2: Keratitis-ichthyosis-deafness syndrome Hereditary lymphedema; Mastocytosis/Urticaria pigmentosa; Hailey–Hailey; ... Read Article
The Pigmentary System. Physiology And Pathophysiology. 2nd ...
Hereditary Sclerosing Poikiloderma Alopecia Areata (Wiete Westerhof). Heterochromia Irides (Wiete Westerhof, David Njoo, & Henk E. Menke). Hemochromatosis and Hemosiderosis (Joerg Albrecht & Victoria P. Werth). Primary Biliary Cirrhosis ... Fetch This Document
Www.barabasilab.com
Alopecia_universalis [704.09] OTHER ALOPECIA 86 Alpers_syndrome [330.8] HEREDITARY DISTURBANCES IN TOOTH STRUCTURE NOT ELS 100 Amish_infantile_epilepsy_syndrome [345.8] Hemochromatosis [275] DISORDERS OF IRON METABOLISM 658 ... Return Document
Www.plosone.org
Neuronopathy, distal hereditary motor, type VI, 604320 (3) Alopecia universalis ?; Atrichia with papular lesions; Congenital atrichia; Hemochromatosis ENSG00000154832 Q9P0U4 brain cancer; pancreatic cancer Breast cancer ... Access This Document
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