从减少的结果

44 B

7 M

948000

389

381

to ~4 options

options split into images, definition, symptoms, related diagnoses, diagnostic tests, therapies, and medications

类别 骨矿代谢, 遗传或先天性 频率 罕见的 (U.S.)

按年龄的可能性

由症状持续时间的可能性

有关医师的类型 family practitioner internist genetics specialist 郵政編碼 找到的地方 結果表明，電腦產生的建議，以幫助您找到一個醫生. MEDgle不推薦任何特定類型的醫生或聲稱是完整或準確的供應商和專業建議.

acromesomelic发育不良 - 型短肢侏儒症 定义 acromesomelic发育不良 http://www.webmd.com/a-to-z-guides/Acromesomelic-Dysplasia 一些常见的症状 有限的手臂动作 四肢短小 身材矮小 一些有关的诊断 1 - 4 of 4 诊断 霍尔特-奥拉姆综合征 enchondromatosis 成骨不全症的类型第三和第四 成骨不全症I型   更多 我有 'acromesomelic发育不良'? 此外，下列诊断测试可能需要帮助核实诊断: 诊断测试的搜索结果 'acromesomelic发育不良' 1 - 4 of 4 诊断测试 透视四肢 acromesomelic发育不良 和 透视四肢 透视脚脚 acromesomelic发育不良 和 透视脚脚 透视手 acromesomelic发育不良 和 透视手 X射线 acromesomelic发育不良 和 X射线 治疗程序为 'acromesomelic发育不良'? 管理或治疗疾病应始终取决于患者的卫生保健提供者. 以下是有关治疗程序或药物 acromesomelic dysplasia: 治疗程序的搜索结果 'acromesomelic发育不良' 1 - 1 of 1 治疗程序 排名是计算机生成的. 请咨询您的卫生保健提供者. 透视脚脚 acromesomelic发育不良 和 透视脚脚 药品的搜索结果 'acromesomelic发育不良' 排名是计算机生成的. 请咨询您的卫生保健提供者. 网络搜索结果 acromesomelic发育不良 网站（所有）  |  治疗  |  药品  |  试验  |  研究  |  饮食 结果 1 - 50 - acromesomelic%26%2321457%3B%26%2332946%3B%26%2319981%3B%26%2333391%3B Acromesomelic Dysplasia [翻译此页] Important It is possible that the main title of the report Acromesomelic Dysplasia is not the name you expected. Please check the synonyms listing to find the ... http://www.webmd.com/a-to-z-guides/acromesomelic-dysplasia   www.webmd.com - summary Acromesomelic dysplasia syndrome(Acromesomelic dysplasia syndrome ... [翻译此页] Disease Acromesomelic dysplasia syndrome (Acromesomelic dysplasia syndrome ... individual study results for: Acromesomelic dysplasia syndrome. No results were found. ... http://www.nextbio.com/b/home/home.nb?q=Acromesomelic+dyspla...   www.nextbio.com - summary Acromesomelic Dysplasia - Yahoo! Health [翻译此页] Important It is possible that the main title of the report Acromesomelic Dysplasia is not the name you expected. Please check the synonyms listing to find the ... http://health.yahoo.com/children-resources/acromesomelic-dys...   health.yahoo.com - summary Orphanet: Acromesomelic dysplasia, Maroteaux type [翻译此页] The portal for rare diseases and orphan drugs ... Acromesomelic dysplasia Maroteaux type (AMDM) is a rare autosomal recessive ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=40   www.orpha.net - summary MIM Morbid map [翻译此页] Acromesomelic dysplasia, Hunter-Thompson type, 201250 (3) GDF5, CDMP1, SYNS2, OS5 ... Acromesomelic dysplasia, Maroteaux type, 602875 (3) NPR2, ANPRB, AMDM ... http://www.ncbi.nlm.nih.gov/Omim/getmorbid.cgi?term=11   www.ncbi.nlm.nih.gov - summary Acromesomelic dysplasia Maroteaux type [翻译此页] Acromesomelic dysplasia Maroteaux type (AMDM) is a rare autosomal recessive ... of an acromesomelic dysplasia on chromosome. 9 by homozygosity mapping. Clin ... http://www.orpha.net/data/patho/GB/uk-acromeso.pdf   www.orpha.net - summary GDF5 - NextBio [翻译此页] GDF5: The protein encoded by this gene is a member of the ... Acromesomelic dysplasia s... Conjugated Linoleic Acid. Chondrocyte. Brachydactyly. Corynanthine ... http://www.nextbio.com/b/home/home.nb?q=GDF5   www.nextbio.com - summary Acromesomelic dysplasia Hunter-Thompson type [翻译此页] Acromesomelic dysplasia Hunter-Thompson type (AMDH) is a very rare autosomal recessive disorder ... acromesomelic dysplasia seems to occur more. rarely than ... http://www.orpha.net/data/patho/GB/uk-hunter05.pdf   www.orpha.net - summary AceView: gene:NPR2, a comprehensive annotation of human, mouse and worm ... [翻译此页] AceView offers a comprehensive annotation of human, mouse and nematode genes reconstructed by co-alignment and clustering ... (Acromesomelic dysplasia, Maroteaux ... http://www.ncbi.nlm.nih.gov/IEB/Research/Acembly/av.cgi?db=human&l=NPR2   www.ncbi.nlm.nih.gov - summary Health Topics aa to ae [翻译此页] ... campomelic Dysplasia. Acanthocheilonemiasis ... Acromesomelic Dwarfism. Acromesomelic Dysplasia. Acromicric Dysplasia. Acromicric Skeletal Dysplasia ... http://www.webmd.com/a-to-z-guides/health-topics/default.htm   www.webmd.com - summary Acromesomelic dysplasia Grebe type [翻译此页] Acromesomelic dysplasia Grebe type (AMDG) is a rare autosomal recessive disorder ... autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and ... http://www.orpha.net/data/patho/Pro/en/AcromesomelicDysplasi...   www.orpha.net - summary MIM Gene map [翻译此页] Acromesomelic dysplasia, Maroteaux type, 602875 (3) REa, A, Fd. 9p21-p12. RMRP, RMRPR, CHH ... dysplasia withouthypotrichosis, 250460 (3); Anauxetic dysplasia, ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l602875   www.ncbi.nlm.nih.gov - summary emailAFriend [翻译此页] Acromesomelic Dysplasia * Indicates required fields. From: Your Name:* Your Email Address: ... Clicking the send button signifies that you have read and agree ... http://www.webmd.com/email_friend?chronicID=091e9c5e8001ee9d   www.webmd.com - summary Gdf5(BP) - NextBio [翻译此页] hide studies that are not seeking new volunteers ... Acromesomelic dysplasia s... Conjugated Linoleic Acid. Chondrocyte. Brachydactyly. Corynanthine ... http://www.nextbio.com/b/home/home.nb?q=BP   www.nextbio.com - summary Orphanet: Acromesomelic dysplasia, Grebe type [翻译此页] The portal for rare diseases and orphan drugs ... Acromesomelic dysplasia Grebe type (AMDG) is a rare autosomal recessive disorder ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=2098   www.orpha.net - summary Health Encyclopedia from A to Z on Yahoo! Health [翻译此页] Health encyclopedia of diseases and conditions covering signs, symptoms, causes, incidence, risk, prevention, tests, diagnosis, treatment, complications and side effects. http://health.yahoo.com/ency/   health.yahoo.com - summary OMIM Update List for March, 2004 [翻译此页] Clinical Synopsis for 201250 ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE ... 135000 FIBROCYSTIC PULMONARY DYSPLASIA ... 213980 CEREBROFACIOTHORACIC DYSPLASIA ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2004   www.ncbi.nlm.nih.gov - summary MIM Gene map [翻译此页] The OMIM Gene map presents the cytogenetic map location of disease genes and ... Acromesomelic dysplasia, Hunter-Thompson type, 201250 (3);Brachydactyly, type C, ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l189971   www.ncbi.nlm.nih.gov - summary A novel member of the STOMATIN/EPB72/mec-2 family, stomatin-like 2 ... [翻译此页] Centre for Functional Genomics and Human Disease, Monash Institute of ... cancers and thought to contain the gene responsible for acromesomelic dysplasia. ... http://www.ncbi.nlm.nih.gov/pubmed/11435687   www.ncbi.nlm.nih.gov - summary A case of chondrodystrophic dwarfism in the Italian late Upper Paleolithic. [翻译此页] During excavations by P. Graziosi at Romito Cave near Papasidero (Cosenza) in ... these features suggests this pathological condition is acromesomelic dysplasia. ... http://www.ncbi.nlm.nih.gov/pubmed/3291617   www.ncbi.nlm.nih.gov - summary AceView: Gene:GDF5, a comprehensive annotation of human, mouse and worm ... [翻译此页] AceView offers a comprehensive annotation of human, mouse and nematode genes reconstructed by co-alignment and ... Acromesomelic dysplasia, Hunter ... http://www.ncbi.nlm.nih.gov/IEB/Research/Acembly/av.cgi?db=h...   www.ncbi.nlm.nih.gov - summary OMIM Update List for February, 2003 [翻译此页] 305620 FRONTOMETAPHYSEAL DYSPLASIA ... Clinical Synopsis for 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM ... SPONDYLOMETAPHYSEAL DYSPLASIA WITH BOWED ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?2.2003   www.ncbi.nlm.nih.gov - summary List of diseases (A) - Wikipedia, the free encyclopedia [翻译此页] Acromesomelic dysplasia Brahimi Bacha type. Acromesomelic dysplasia Campailla ... Acromesomelic dysplasia. Acromicric dysplasia. Acroosteolysis dominant type ... http://en.wikipedia.org/wiki/List_of_diseases_(A)   en.wikipedia.org - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juillet ... [翻译此页] ... 3 0.01% campailla-martinelli-type acromesomelic dwarfism 3 0.01% camptocormia 3 ... 0.01% arrhythmogenic right ventricular dysplasia 2 0.01% arteria ombelicale ... http://orphanet.orpha.net/stat/orphanet/search_200607.html   orphanet.orpha.net - summary OMIM Update List for February, 2009 [翻译此页] 248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA ... Clinical Synopsis for 201250 ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?2.2009   www.ncbi.nlm.nih.gov - summary OMIM Update List for June, 2004 [翻译此页] 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM. 603137 CULLIN 4A; CUL4A ... Clinical Synopsis for 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?6.2004   www.ncbi.nlm.nih.gov - summary MIM Gene map [翻译此页] The OMIM Gene map presents the cytogenetic map location of disease genes and ... Acromesomelic dysplasia, Hunter-Thompson type, 201250 (3);Brachydactyly, type C, ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?chromosome=20q12   www.ncbi.nlm.nih.gov - summary O Habbal - NextBio [翻译此页] Clinical and molecular analysis of Grebe acromesomelic dysplasia in an Omani family. ... Grebe syndrome is a rare autosomal recessive acromesomelic dysplasia. ... http://www.nextbio.com/b/literature/literature.nb?author=O+Habbal   www.nextbio.com - summary 201250 [翻译此页] http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=201250   www.ncbi.nlm.nih.gov - summary NextBio: Clinical and molecular analysis of Grebe acromesomelic ... [翻译此页] ... and molecular analysis of Grebe acromesomelic dysplasia in an Omani family. ... acromesomelic dysplasia axial skeletons carpal bones fifth finger Grebe syndrome ... http://www.nextbio.com/b/literature/literature.nb?id=1290089...   www.nextbio.com - summary GDF5 - Wikipedia, the free encyclopedia [翻译此页] ... are associated with acromesomelic dysplasia, Hunter-Thompson type; brachydactyly, ... gene and severe acromesomelic chondrodysplasia resembling Grebe-type ... http://en.wikipedia.org/wiki/GDF5   en.wikipedia.org - summary OMIM Update List for October, 1997 [翻译此页] ... RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1. 112250 BONE DYSPLASIA WITH MEDULLARY FIBROSARCOMA ... 201250 ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?10.1997   www.ncbi.nlm.nih.gov - summary OMIM Update List for October, 2002 [翻译此页] 271510 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE ... Clinical Synopsis for 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?10.2002   www.ncbi.nlm.nih.gov - summary Children's Health: Other Resources - Yahoo! Health [翻译此页] Find information on children's health including immunizations, behavior & development, injuries & safety, ... 50. Acromesomelic Dysplasia. Article. 09/23 ... http://health.yahoo.com/children-resources/   health.yahoo.com - summary OMIM Update List for March, 2002 [翻译此页] 604292 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME ... Clinical Synopsis for 201250 ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2002   www.ncbi.nlm.nih.gov - summary Tarsal bone - NextBio [翻译此页] ... causes a new subtype of acromesomelic chondrodysplasia with genital anomalies. ... Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3. ... http://www.nextbio.com/b/home/home.nb?q=tarsal+bone   www.nextbio.com - summary OMIM Update List for July, 1998 [翻译此页] 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE. 602885 G ... 201250 ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE. 215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?7.1998   www.ncbi.nlm.nih.gov - summary OMIM Update List for August, 1998 [翻译此页] 314300 TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR ... 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM. August 7, 1998. New Entries: ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?8.1998   www.ncbi.nlm.nih.gov - summary OMIM Update List for August, 2002 [翻译此页] Clinical Synopsis for 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM ... 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?8.2002   www.ncbi.nlm.nih.gov - summary OMIM Update List for September, 1997 [翻译此页] 174810 POLYOSTOTIC OSTEOLYTIC DYSPLASIA, HEREDITARY EXPANSILE; HEPOD ... 201250 ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE. 208900 ATAXIA-TELANGIECTASIA; AT ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?9.1997   www.ncbi.nlm.nih.gov - summary 108961 [翻译此页] http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108961   www.ncbi.nlm.nih.gov - summary 602875 [翻译此页] http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602875   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Octobre ... [翻译此页] ... rett 12 0.02% right ventricular dysplasia 12 0.02% salmonelose 12 0.02% seckel ... demencia fronto-temporal 3 0.01% dentin dysplasia type 2 3 0.01% dentina 3 0.01 ... http://www.orpha.net/stat/orphanet/search_200610.html   www.orpha.net - summary B Zabel - NextBio [翻译此页] acromesomelic dysplasia amino acids Beckwith-Wiedemann syndrome chondrocyte ... NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux. ... http://www.nextbio.com/b/literature/literature.nb?author=B+Zabel   www.nextbio.com - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Fevrier ... [翻译此页] ... estenosis pulmonar 8 0.01% facial dysplasia 8 0.01% gitelman 8 0.01 ... metilcobalamina 4 0.01% meyer's dysplasia 4 0.01% microcefalia bilaterale 4 ... http://www.orpha.net/stat/orphanet/search_200702.html   www.orpha.net - summary OMIM Update List for November, 2008 [翻译此页] 201250 ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE ... 610839 OSTEOARTHRITIS, GENERALIZED, WITHOUT DYSPLASIA; GOA1 ... 231050 GELEOPHYSIC DYSPLASIA ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?11.2008   www.ncbi.nlm.nih.gov - summary DS Kumar - NextBio [翻译此页] Clinical and molecular analysis of Grebe acromesomelic dysplasia in an Omani family. ... Grebe syndrome is a rare autosomal recessive acromesomelic dysplasia. ... http://www.nextbio.com/b/literature/literature.nb?author=DS+Kumar   www.nextbio.com - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Mai 2008 - URL [翻译此页] Généré le 01-Jun-2008 22:39 CEST. Hits Ko URL -978818 6.61% 13973810 5.30 ... ectodermal-dysplasia-anhidrotic.pdf 319 0.00% 14855 0.01% /data/patho/FR/fr ... http://www.orpha.net/stat/orphanet/url_200805.html   www.orpha.net - summary OMIM Update List for February, 2001 [翻译此页] 132400 EPIPHYSEAL DYSPLASIA, MULTIPLE, 1; EDM1 ... 602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM ... LANGER MESOMELIC DYSPLASIA. 304800 DIABETES ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?2.2001   www.ncbi.nlm.nih.gov - summary OMIM Update List for April, 2003 [翻译此页] 215140 HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA ... Clinical Synopsis for 201250 ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?4.2003   www.ncbi.nlm.nih.gov - summary 显示更多 1  2