Reproductive Genetics Institute (RGI)
Alopecia universalis congenita; alzheimer disease 4 psen2 amyloidosis i, hereditary neuropathic ttr amyotrophic lateral sclerosis 1; als1 sod1 androgen receptor; ar (testicular feminization; spastic paraplegia 3, autosomal dominant atl1 spastic paraplegia 4, autosomal dominant; ... Read More
Hospital Outpatient Activity - April 2010 - March 2011 ...
Hereditary spastic paraplegia Hereditary ataxia, unspecified Motor neuron disease Other spinal muscular atrophies and related syndromes Alopecia universalis Other alopecia areata Alopecia areata, unspecified Androgenic alopecia, unspecified Telogen effluvium ... Doc Viewer
Www.barabasilab.com
Alopecia_universalis [704.09] OTHER ALOPECIA 86 Alpers_syndrome [330.8] OTHER SPECIFIED CEREBRAL DEGENERATIONS IN CHILDHOO 87 HEREDITARY SPASTIC PARAPLEGIA 957 MASS_syndrome 958 Mast_cell_leukemia 959 Mastocytosis_with_associated_hematologic_disorder 960 Mast_syndrome ... Document Viewer
Genetic Disorders In Arab Populations Indexed In The CTGA ...
182601 Spastic Paraplegia 4, Autosomal Dominant T 182860 Spectrin, Alpha, Hereditary Hemorrhagic, of Rendu, Osler, and Weber A B 187400 Testicular Torsion B Sa 203655 Alopecia Universalis Congenita O ... Fetch Full Source
The Human Disease Network - CCNR
Alopecia universalis Alpers syndrome 87 Alpha-actinin-3 deficiency 92 Alport syndrome hereditary benign 320 Chudley-Lowry syndrome 329 Chylomicron retention disease Ciliary dyskinesia 1396 Silver spastic paraplegia syndrome 1383 Severe combined immunodeficiency ... Document Viewer
Steatocystoma Multiplex - Wikipedia, The Free Encyclopedia
(Redirected from Hereditary epidermal polycystic disease) Jump to: navigation, Frontal fibrosing alopecia; Marie Unna hereditary hypotrichosis; Hypertrichosis: Hirsutism; Acquired localised; Hereditary spastic paraplegia 10; Dynein: Primary ciliary dyskinesia; ... Read Article
Bioinformatics.oxfordjournals.org
Spastic_ataxia/paraplegia TABES DORSALIS Mucoepidermoid_salivary_gland_carcinoma MALIGNANT NEOPLASM OF SALIVARY GLAND UNSPECIFIED Salivary_adenoma Nasopharyngeal_carcinoma MALIGNANT NEOPLASM OF NASOPHARYNX UNSPECIFIED SITE Esophageal_cancer ... Get Content Here
ID Panel Indikationen 120614 - MedUni Wien: Startseite
O Alopecia Universalis Congenita (ALUNC) HR O Hereditary Hemorrhagic Telangiectasia ENG O Long/Short QT Syndrome, O Spastic Paraplegia SPG7, KIAA0196, L1CAM, ATL1 O Spinocerebellar Ataxia ATXN1, ATXN2, ATXN7 O ... Fetch This Document
Hereditary Palmoplantar Keratosis - InTech
Hereditary Palmoplantar Keratosis congenital alopecia universalis, pseudopelade type alopecia, acanthosis nigricans, spastic paraplegia, myopathy, nail changes, mental retardation, bullous lesions on the soles, and seizures [4]. ... View Document
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 1396Silver spastic paraplegia syndrome 1383Severe combined immunodeficiency ... Access Document
Hereditary Palmoplantar Keratosis - InTech
58 Current Genetics in Dermatology reported findings are deaf-mutism, congenital alopecia universalis, pseudopelade type alopecia, acanthosis nigricans, spastic paraplegia, myopathy, nail changes, mental ... Get Content Here
Ion AmpliSeq™ Inherited Disease Panel Target Gene List
Ion AmpliSeq ™ Inherited Disease Panel target gene list Symbol Disease ATL1 Spastic Paraplegia-3A ATM Ataxia-Telangiectasia ATP2A2 Darier Disease ENG Hereditary Hemorrhagic Telangiectasia EXT1 Exostoses, Multiple, Type 1 ... Access Content
Www.nature.com
Spastic paraplegia 31, 610250 (3) RFX5 Neuropathy, hereditary sensory, with spastic paraplegia, 256840 (3) CD151,PETA3,SFA1,MER2 Alopecia universalis, 203655 (3); Atrichia with papular lesions,209500 (3); Hypotrichosis, hereditary, ... Get Document
Book C, Supplement No. 30 - Veterans Benefits Administration Home
Schedule for Rating Disabilities. Veterans Benefits Alopecia: Areata 7831 4.118. Scarring 7830 Paraplegia with loss of use of both lower extremities and loss of anal and bladder sphincter control qualifies for subpar. O. Code O-2 (38 CFR 3.350(e)(2). Where there are additional ... Return Document
Auftrag Zur DNA Panel Diagnostik Ion AmpliSeq™ Inherited ...
Ion AmpliSeq™ Inherited Disease Panel O Alopecia Universalis Congenita (ALUNC) - HR O O Spastic Paraplegia Type 1 ‐ L1 Syndrome - L1CAM O ... Read Full Source
Ftp.cdc.gov
Drug-induced androgenic alopecia Lead-induced gout Drug-induced gout Kaschin-Beck disease Polyarteritis with lung involvement [Churg-Strauss] Immunodeficiency following hereditary defective response to Epstein-Barr virus ... Retrieve Doc
Www.gov.uk
Hereditary hypogammaglobulinaemia D801 Nonfamilial hypogammaglobulinaemia D802 Selective deficiency of immunoglobulin A [IgA] D803 Selective deficiency of immunoglobulin G [IgG] subclasses D804 Selective deficiency of immunoglobulin M [IgM] D805 ... Retrieve Content
BoardII RevNotes - SP-01
Alopecia universalis - hair loss over entire body. Hirsuitism - excessive hair growth in unusual places, especially in women. Spastic paralysis Flaccid paralysis. hereditary, trauma, 50% have a Hx of significant trauma. endocrine, inflammatory, ... Get Document
8. Case Report Vohwinkel Syndrome - JPAD - Journal Of ...
Case report Vohwinkel’s syndrome: Case report and • Congenital alopecia universalis • Pseudopelade-type alopecia • High-tone acoustic impairment • Ichthyosiform dermatitis • Spastic paraplegia/myopathy • Nail changes • Mental retardation • Bullae on ... Content Retrieval
Prevalence Of Rare Diseases: Bibliographic Data
X rare disease mean duration ; 701 Alopecia universalis 25 94058 Neovascular glaucoma 24.4 1199 Esophageal atresia 24.3 3318 Essential thrombocythemia 24 685 Hereditary spastic paraplegia 5 2189 Hydrolethalus 5** 35099 Isolated brachycephaly 5 ... Read More
Www.plosgenetics.org
Hyperekplexia, hereditary lacrimoauriculodentodigital syndrome; ladd ... Document Viewer
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