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metaphyseal chondrodysplasia schmid type - inherited disorder causing bowed limbs and short stature
Definition for metaphyseal chondrodysplasia Schmid type
http://health.yahoo.com/ency/healthwise/nord960
some common symptoms
abnormal gait
bowed limbs
pain in leg(s)
short stature
some related diagnoses
1 - 7 of
11
diagnoses
osteochondroma
osteomalacia
osteoarthritis
celiac disease
malabsorption
syphilis
osteogenesis imperfecta types III and IV
more
do i have 'metaphyseal chondrodysplasia Schmid type'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'metaphyseal chondrodysplasia schmid type'
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diagnostic tests
Molecular Genetic Studies
metaphyseal chondrodysplasia Schmid type and Molecular Genetic Studies
Skeletal radiograph survey
metaphyseal chondrodysplasia Schmid type and Skeletal radiograph survey
X-ray pelvis
metaphyseal chondrodysplasia Schmid type and X-ray pelvis
X-ray spine
metaphyseal chondrodysplasia Schmid type and X-ray spine
X-ray foot (feet)
metaphyseal chondrodysplasia Schmid type and X-ray foot (feet)
X-ray hand(s)
metaphyseal chondrodysplasia Schmid type and X-ray hand(s)
X-ray skull
metaphyseal chondrodysplasia Schmid type and X-ray skull
Chorionic Villus Sampling (CVS)
metaphyseal chondrodysplasia Schmid type and Chorionic Villus Sampling (CVS)
Prenatal Ultrasound
Ultrasound on the fetus before birth
metaphyseal chondrodysplasia Schmid type and Prenatal Ultrasound
X-rays
metaphyseal chondrodysplasia Schmid type and X-rays
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therapeutic procedures for 'metaphyseal chondrodysplasia Schmid type'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for metaphyseal chondrodysplasia Schmid type:
therapeutic procedure search results for 'metaphyseal chondrodysplasia schmid type'
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Orthopedic surgical care
metaphyseal chondrodysplasia Schmid type and Orthopedic surgical care
X-ray foot (feet)
metaphyseal chondrodysplasia Schmid type and X-ray foot (feet)
medications search results for 'metaphyseal chondrodysplasia schmid type'
rankings are computer generated. please consult your health care provider.
web search results for metaphyseal chondrodysplasia schmid type
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- metaphyseal chondrodysplasia Schmid type
Metaphyseal Chondrodysplasia, Schmid Type - Yahoo! Health
Important It is possible that the main title of the report Metaphyseal Chondrodysplasia, Schmid Type is not the name you expected. Please check the synonyms listing ...
http://health.yahoo.com/musculoskeletal-resources/metaphysea...
health.yahoo.com
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summary
Orphanet: Metaphyseal chondrodysplasia, Schmid type
Metaphyseal chondrodysplasia, Schmid type. Orpha number. ORPHA174. Prevalence of rare diseases ... Schmid metaphyseal chondrodysplasia is a rare disorder ...
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=174
www.orpha.net
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Schmid metaphyseal chondrodysplasia - Wikipedia, the free encyclopedia
Schmid type of metaphyseal chondrodysplasia and COL10A1 mutations--findings in 10 patients" ... human and mouse metaphyseal chondrodysplasia type Schmid". Hum. ...
http://en.wikipedia.org/wiki/Schmid_metaphyseal_chondrodysplasia
en.wikipedia.org
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A type X collagen mutation causes Schmid metaphyseal chondrodysplasia.
The expression of type X collagen is restricted to hypertrophic chondrocytes in ... dominant Schmid metaphyseal chondrodysplasia in a large Mormon kindred (lod ...
http://www.ncbi.nlm.nih.gov/pubmed/8220429
www.ncbi.nlm.nih.gov
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Jansen's metaphyseal chondrodysplasia - Wikipedia, the free encyclopedia
METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE GenomeNet ... Metaphyseal dysplasia · Jansen's metaphyseal chondrodysplasia · Schmid ...
http://en.wikipedia.org/wiki/Jansen's_metaphyseal_chondrodysplasia
en.wikipedia.org
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Concentration of mutations causing Schmid metaphyseal chondrodysplasia ...
... chondrodysplasia in the C-terminal noncollagenous domain of type X collagen. ... Schmid metaphyseal chondrodysplasia (SMCD) has previously been shown to be the ...
http://www.ncbi.nlm.nih.gov/pubmed/7749409
www.ncbi.nlm.nih.gov
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WebMD Health A-Z - Find reliable health and medical information on ...
Find a comprehensive index of trusted health and medical information. It is your ultimate guide to reliable ... Metaphyseal Chondrodysplasia Schmid Type ...
http://www.webmd.com/a-to-z-guides/health-topics/ma-me.htm
www.webmd.com
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COL10A1 - NextBio
... This gene encodes the alpha chain of type X collagen, a short chain collagen expressed by ... Schmid type metaphyseal chondrodysplasia (SMCD) and Japanese type ...
http://www.nextbio.com/b/home/home.nb?q=COL10A1
www.nextbio.com
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Osteochondrodysplasia - Wikipedia, the free encyclopedia
Metaphyseal dysplasia · Jansen's metaphyseal chondrodysplasia · Schmid ... Achondrogenesis (type 2) · Hypochondrogenesis. SLC26A2 sulfation defect ...
http://en.wikipedia.org/wiki/Osteochondrodysplasia
en.wikipedia.org
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156500
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156500
www.ncbi.nlm.nih.gov
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Osteochondrodysplasias: Bone and Connective Tissue Disorders in ...
Peroxisomal type 2 targeting signal receptor (PTS2) ... Metaphyseal chondrodysplasia.? In some forms, malabsorption, neutropenia, thymolymphopenia ...
http://www.merck.com/mmpe/print/sec19/ch284/ch284k.html
www.merck.com
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PMID 8782043
... metaphyseal chondrodysplasia type Schmid but not several other forms of ... been identified in subjects with metaphyseal chondrodysplasia type Schmid (MCDS) ...
http://www.ncbi.nlm.nih.gov/pubmed/8782043
www.ncbi.nlm.nih.gov
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Atelosteogenesis, type II - Wikipedia, the free encyclopedia
Metaphyseal dysplasia · Jansen's metaphyseal chondrodysplasia · Schmid metaphyseal chondrodysplasia ... Achondrogenesis (type 2) · Hypochondrogenesis. SLC26A2 ...
http://en.wikipedia.org/wiki/Atelosteogenesis,_type_II
en.wikipedia.org
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Osteochondrodysplasias: Bone and Connective Tissue Disorders in ...
Peroxisomal type 2 targeting signal receptor (PTS2) ... Metaphyseal chondrodysplasia.? In some forms, malabsorption, neutropenia, thymolymphopenia ...
http://www.merck.com/mmpe/sec19/ch284/ch284k.html
www.merck.com
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summary
Amino acid substitutions of conserved residues in the carboxyl-terminal ...
... of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid. ... individuals with metaphyseal chondrodysplasia type ...
http://www.ncbi.nlm.nih.gov/pubmed/8304336
www.ncbi.nlm.nih.gov
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PMID 9067753
... type X collagen gene (COL10A1) in patients with Schmid metaphyseal chondrodysplasia. 131-5 Schmid metaphyseal chondrodysplasia (SMCD) is a relatively common, ...
http://www.ncbi.nlm.nih.gov/pubmed/9067753
www.ncbi.nlm.nih.gov
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Spondyloepimetaphyseal dysplasia - Wikipedia, the free encyclopedia
COL2: Hypochondrogenesis · Achondrogenesis type 2 · Stickler syndrome · Marshall ... COL10: Schmid metaphyseal chondrodysplasia ...
http://en.wikipedia.org/wiki/Spondyloepimetaphyseal_dysplasia,_Strudwick_type
en.wikipedia.org
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MIM Gene map
Metaphyseal chondrodysplasia, Schmid type (3); Spondylometaphysealdysplasia, Japanese type (3) ... Nephropathy, IgA type (2) Fd. Copyright © 1966-2009 Johns ...
http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?chromosome=6q21
www.ncbi.nlm.nih.gov
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MIM Gene map
Metaphyseal chondrodysplasia, Schmid type (3); Spondylometaphysealdysplasia, Japanese type (3) ... Nephropathy, IgA type (2) Fd. 6q22-q23. LAMA2, LAMM. Laminin, ...
http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?d4047
www.ncbi.nlm.nih.gov
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Collagenopathy, types II and XI - Wikipedia, the free encyclopedia
spondyloepimetaphyseal dysplasia, Strudwick type. spondyloepiphyseal dysplasia congenita ... COL10: Schmid metaphyseal chondrodysplasia ...
http://en.wikipedia.org/wiki/Collagenopathy,_types_II_and_XI
en.wikipedia.org
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MIM Gene map
Metaphyseal chondrodysplasia, Schmid type (3); Spondylometaphysealdysplasia, Japanese type (3) ... Nephropathy, IgA type (2) Fd. 6q22-q23. LAMA2, LAMM. Laminin, ...
http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l603423
www.ncbi.nlm.nih.gov
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MIM Gene map
Metaphyseal chondrodysplasia, Schmid type (3); Spondylometaphysealdysplasia, Japanese type (3) ... 164200 (3); Syndactyly, type III,186100 (3); Hypoplastic ...
http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l609758
www.ncbi.nlm.nih.gov
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PMID 8004099
... type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locus. ... to segregate with Schmid metaphyseal chondrodysplasia, an autosomal dominant ...
http://www.ncbi.nlm.nih.gov/pubmed/8004099
www.ncbi.nlm.nih.gov
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Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Mars 2007 ...
... 13 0.02% cetoacidose 13 0.02% chondrodysplasia punctata 13 0.02% collagenous ... bowen-conradi syndrome 5 0.01% brachydactyly type d 5 0.01% brugada syndrome ekg ...
http://orphanet.orpha.net/stat/orphanet/search_200703.html
orphanet.orpha.net
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MIM Gene map
Metaphyseal chondrodysplasia, Schmid type (3); Spondylometaphysealdysplasia, Japanese type (3) ... Nephropathy, IgA type (2) Fd. 6q22-q23. LAMA2, LAMM. Laminin, ...
http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?d4044
www.ncbi.nlm.nih.gov
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Metaphyseal Chondrodysplasia, Schmid Type
Important It is possible that the main title of the report Metaphyseal Chondrodysplasia, Schmid Type is not the name you expected. ...
http://www.webmd.com/children/Metaphyseal-Chondrodysplasia-Schmid-Type
www.webmd.com
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WG Cole - NextBio
... plate in human and mouse metaphyseal chondrodysplasia type Schmid. ... BACKGROUND: The Schmid type of metaphyseal chondrodysplasia (MCDS) is generally ...
http://www.nextbio.com/b/literature/literature.nb?author=WG+Cole
www.nextbio.com
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Orphanet: Diseases list
Metaphyseal chondrodysplasia - retinitis pigmentosa. Metaphyseal chondrodysplasia, Schmid type. Metaphyseal chondrodysplasia, Spahr type ...
http://www.orpha.net/consor/cgi-bin/Disease_Search_List.php?lng=EN&TAG=M
www.orpha.net
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Collagen, type X, alpha 1 (COL10A1)
Human protein-coding gene COL10A1. Represented by 35 ESTs from 23 cDNA libraries. ... {C-terminal} [human, metaphyseal chondrodysplasia type Schmid patient, mRNA ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=520339
www.ncbi.nlm.nih.gov
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PMID 16838329
... (CHH) or McKusick type metaphyseal chondrodysplasia (MCD) (OMIM # 250250) is ... of these patients, the diagnosis of Schmid type MCD (OMIM # 156500) was made and ...
http://www.ncbi.nlm.nih.gov/pubmed/16838329
www.ncbi.nlm.nih.gov
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Type X collagen multimer assembly in vitro is prevented by a Gly618 to ...
... alpha 1(X) NC1 domain resulting in Schmid metaphyseal chondrodysplasia. ... a family with Schmid metaphyseal chondrodysplasia demonstrated that the affected ...
http://www.ncbi.nlm.nih.gov/pubmed/7876225
www.ncbi.nlm.nih.gov
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A novel mutation substituting tryptophan with arginine in the carboxyl ...
... identified in a Japanese family with Schmid metaphyseal chondrodysplasia (SMCD) ... in type X collagens, and 4, the mutation causes a marked change in the ...
http://www.ncbi.nlm.nih.gov/pubmed/8554571
www.ncbi.nlm.nih.gov
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Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Aout 2006 ...
... fibrosis pulmonar 11 0.03% gitelman 11 0.03% glycogen storage disease type 1a ... 9 0.02% chondrodysplasia punctata 9 0.02% collagenous colitis more: ...
http://www.orpha.net/stat/orphanet/search_200608.html
www.orpha.net
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PMID 8986632
Dideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and ... 112-7 Schmid metaphyseal chondrodysplasia (SMCD; MIM 156500) is an autosomal ...
http://www.ncbi.nlm.nih.gov/pubmed/8986632
www.ncbi.nlm.nih.gov
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Sack-Barabas syndrome - Wikipedia, the free encyclopedia
COL2: Hypochondrogenesis · Achondrogenesis type 2 · Stickler syndrome · Marshall ... COL10: Schmid metaphyseal chondrodysplasia ...
http://en.wikipedia.org/wiki/Ehlers-Danlos_syndrome,_vascular_type
en.wikipedia.org
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Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Septembre ...
tumeur stromale 5 0.01% type 4 hyperlipidemia 5 0.01% types of biliary atresia 5 ... 0.01% rhizomelic chondrodysplasia punctata 4 0.01% rhumatisme articulaire aigu 4 ...
http://www.orpha.net/stat/orphanet/search_200609.html
www.orpha.net
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OMIM Update List for October, 2005
606843 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 3 ... for 609441 CHONDRODYSPLASIA, ACROMESOMELIC, WITH ... 156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS ...
http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?10.2005
www.ncbi.nlm.nih.gov
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OMIM Update List for November, 2004
156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS ... 118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE. 119530 OROFACIAL CLEFT 1; OFC1 ...
http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?11.2004
www.ncbi.nlm.nih.gov
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Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Fevrier ...
... camptodactilia 20 0.03% carcinoma papillare 20 0.03% chondrodysplasia punctata ... hyperglycinemia 5 0.01% hyperlipidemia type 4 5 0.01% hypertrichosis lanuginosa ...
http://www.orpha.net/stat/orphanet/search_200702.html
www.orpha.net
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OMIM Update List for February, 2005
130000 EHLERS-DANLOS SYNDROME, TYPE I ... for 250420 METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, ... 156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS ...
http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?2.2005
www.ncbi.nlm.nih.gov
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List of diseases (M) - Wikipedia, the free encyclopedia
McKusick type metaphyseal chondrodysplasia. McLain Debakian syndrome. McPherson Clemens ... Metaphyseal anadysplasia. Metaphyseal chondrodysplasia Schmid type ...
http://en.wikipedia.org/wiki/List_of_diseases_(M)
en.wikipedia.org
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OMIM Update List for June, 2005
... CHONDRODYSPLASIA, ACROMESOMELIC, ... 609162 CZECH DYSPLASIA, METATARSAL TYPE ... Clinical Synopsis for 156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS ...
http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?6.2005
www.ncbi.nlm.nih.gov
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11839302
Mutations in the NC1 domain cause Schmid metaphyseal chondrodysplasia (SMCD) ... Collagen Type X chemistry genetics Crystallography, X-Ray Exostoses, Multiple ...
http://www.ncbi.nlm.nih.gov/pubmed/11839302
www.ncbi.nlm.nih.gov
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Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Avril 2007 ...
... higashi 9 0.01% cholesterol biosynthesis 9 0.01% chondrodysplasia punctata 9 ... comun variable 5 0.01% jansen metaphyseal dysplasia 5 0.01% klippel feil 5 ...
http://www.orpha.net/stat/orphanet/search_200704.html
www.orpha.net
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Deletions in the COL10A1 gene are not associated with skeletal changes ...
Type 10 collagen alpha 1 (COL10A1) is a short-chain collagen of cartilage ... metaphyseal chondrodysplasia (SMCD), a cartilage disorder characterized by short ...
http://www.ncbi.nlm.nih.gov/pubmed/16845471
www.ncbi.nlm.nih.gov
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PMID 8012364
... mutation in type X collagen in a family with Schmid metaphyseal chondrodysplasia. 507-9 Department of Medicine, Thomas Jefferson University, Philadelphia, PA ...
http://www.ncbi.nlm.nih.gov/pubmed/8012364
www.ncbi.nlm.nih.gov
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Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Mars 2008 ...
... pigmentada 3 0.01% sintesis de schmid's 3 0.01% sintrome turner 3 0.01 ... 2 0.00% brachytelephalangic type chondrodysplasia punctata 2 0.00% bradykinà ...
http://www.orpha.net/stat/orphanet/search_200803.html
www.orpha.net
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Metaphyseal chondrodysplasia, Schmid type
http://www.nextbio.com/b/home/home.nb?q=Metaphyseal+chondrod...
www.nextbio.com
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OMIM Update List for March, 2007
... CHANNEL, VOLTAGE-GATED, TYPE III, BETA SUBUNIT; SCN3B ... IMPERFECTA, TYPE VII ... 156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS. 171880 ...
http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2007
www.ncbi.nlm.nih.gov
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Collagen, type X, alpha 1 - Wikipedia, the free encyclopedia
Collagen, type X, alpha 1(Schmid metaphyseal chondrodysplasia), also known as ... metaphyseal chondrodysplasia type Schmid but not several other forms of ...
http://en.wikipedia.org/wiki/COL10A1
en.wikipedia.org
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