- Chondrocalcinosis
, hypophosphatemia , hypomagnesemia and renal osteodystrophy are often also associated with chondrocalcinosis ... more details
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- List of ICD-9 codes 240?279: endocrine, nutritional and metabolic diseases, and immunity disorders
Familial hypophosphatemia Hypophosphatasia ICD9 275.4 Disorders of calcium metabolism ICD9 ... more details
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- Orthopantomogram
, hypophosphatemia, The most common use is to determine the status of wisdom teeth and trauma to the jaws ... more details
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- List of MeSH codes (C16)
For other categories, see List of MeSH codes . The following is a list of the C codes for MeSH . It is a product of the United States National Library of Medicine . Source for content is http www.nlm.nih.gov mesh filelist.html here . File 2006 MeSH Trees . MeshNumber C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities congenital, hereditary, and neonatal diseases and abnormalities MeshNumber C16.131 Abnormalities abnormalities MeshNumber C16.131.042 Abnormalities, Drug Induced abnormalities, drug induced MeshNumber C16.131.077 Abnormalities, Multiple abnormalities, multiple MeshNumber C16.131.077.065 Alagille Syndrome alagille syndrome MeshNumber C16.131.077.095 Angelman Syndrome angelman syndrome MeshNumber C16.131.077.112 Bardet Biedl Syndrome bardet biedl syndrome MeshNumber C16.131.077.130 Basal Cell Nevus Syndrome basal cell nevus syndrome MeshNumber C16.131.077.133 Beckwith Wiedemann Syndrome beckwith wiedemann syndrome MeshNumber C16.131.077.137 Bloom Syndrome bloom syndrome MeshNumber C16.131.077.208 Branchio Oto Renal Syndrome Branchio Oto Renal Syndrome branchio oto renal syndrome MeshNumber C16.131.077.250 Cockayne Syndrome cockayne syndrome MeshNumber C16.131.077.262 Cri du Chat Syndrome cri du chat syndrome MeshNumber C16.131.077.272 De Lange Syndrome de lange syndrome MeshNumber C16.131.077.327 Down Syndrome down syndrome MeshNumber C16.131.077.350 Ectodermal Dysplasia ectodermal dysplasia MeshNumber C16.131.077.350.398 Ellis Van Creveld Syndrome ellis van creveld syndrome MeshNumber C16.131.077.350.424 Focal Dermal Hypoplasia focal dermal hypoplasia MeshNumber C16.131.077.350.712 Neurocutaneous Syndromes neurocutaneous syndromes MeshNumber C16.131.077.393 Gardner Syndrome gardner syndrome MeshNumber C16.131.077.410 Holoprosencephaly holoprosencephaly MeshNumber C16.131.077.445 Incontinentia Pigmenti incontinentia pigmenti MeshNumber C16.131.077.509 Laurence Moon Syndrome laurence moon syndrome MeshNumber C16.131.077.525 LEOPARD Syndrom ... more details
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- DMP1 (gene)
Orphan date February 2009 PBB geneid 1758 Dentin matrix acidic phosphoprotein 1 is a protein that in humans is encoded by the DMP1 gene . ref name pmid8586437 cite journal author Aplin HM, Hirst KL, Crosby AH, Dixon MJ title Mapping of the human dentin matrix acidic phosphoprotein gene DMP1 to the dentinogenesis imperfecta type II critical region at chromosome 4q21 journal Genomics volume 30 issue 2 pages 347 9 year 1996 month Mar pmid 8586437 pmc doi 10.1006 geno.1995.9867 ref ref name pmid9177774 cite journal author Hirst KL, Simmons D, Feng J, Aplin H, Dixon MJ, MacDougall M title Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein 1 DMP1 gene exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II journal Genomics volume 42 issue 1 pages 38 45 year 1997 month Jul pmid 9177774 pmc doi 10.1006 geno.1997.4700 ref ref name entrez The PBB Summary template is automatically maintained by Protein Box Bot. See Template PBB Controls to Stop updates. PBB Summary section title summary text Dentin matrix acidic phosphoprotein is an extracellular matrix protein and a member of the small integrin binding ligand N linked glycoprotein family. This protein, which is critical for proper mineralization of bone and dentin, is present in diverse cells of bone and tooth tissues. The protein contains a large number of acidic domains, multiple phosphorylation sites, a functional arg gly asp cell attachment sequence, and a DNA binding domain. In undifferentiated osteoblasts it is primarily a nuclear protein that regulates the expression of osteoblast specific genes. During osteoblast maturation the protein becomes phosphorylated and is exported to the extracellular matrix, where it orchestrates mineralized matrix formation. Mutations in the gene are known to cause autosomal recessive hypophosphatemia, a disease that manifests as rickets and osteomalacia. The gene structure is conserved in ... more details
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- Schimmelpenning syndrome
rickets and hypophosphatemia. Cardiovascular abnormalities include ventricular septal defect and co ... more details
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- Cholecalciferol
is tightly regulated stimulated by either parathyroid hormone or hypophosphatemia and serves as the major ... more details
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- Urinalysis
and secondary types. Primary hypophosphatemia is characterized by direct excess excretion of phosphate ... more details
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- Transthyretin
10 pages 1043 1047 last Marik first P. E. coauthors M. K. Bedigian title Refeeding hypophosphatemia ... more details
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- Hypomagnesemia
, which is also increased because of alcoholic and diabetic ketoacidosis , hypophosphatemia ... more details
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- Organic anion transporter 1
in the setting of normal serum glucose levels, phosphate wasting with hypophosphatemia, proteinuria ... more details
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- Dietary mineral
work accessdate 2008 11 29 ref hypophosphatemia hyperphosphatemia Magnesium span style display ... more details
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- Phosphorus
. All are characterized by hypophosphatemia , which is a condition of low levels of soluble phosphate levels in the blood serum, and therefore inside cells. Symptoms of hypophosphatemia include muscle ... more details
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- Psychosis
and Related Sciences volume 34 issue 2 pages 122 125 pmid 9231574 ref and hypophosphatemia ... aspect of hypophosphatemia journal Canadian Journal of Psychiatry volume 29 issue 7 pages 599 ... more details
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- David Blaine
have alerted us to the risks of refeeding. Despite cautious management, he had hypophosphatemia ... more details
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- Rhabdomyolysis
levels , hypophosphatemia low phosphate levels , ketoacidosis e.g. in diabetic ketoacidosis or hypothyroidism ... more details
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- Osteopontin
S0092 8674 00 80257 3 url issn ref Hypocalcemia and hypophosphatemia instances that stimulate ... more details
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- Gluten-sensitive enteropathy associated conditions
abnormalities. Iron Iron deficiency anemia Phosphorus hypophosphatemia, ref name pmid7216140 ... more details
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- Hypovitaminosis D
due to genetic disorders such as autosomal dominant hypophosphatemic rickets or X linked hypophosphatemia ... more details
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- Primidone
drugbox verifiedrevid 420325519 IUPAC name 5 ethyl 5 phenyl hexahydropyrimidine 4,6 dione image Primidone structure.svg width 127 CASNo Ref cascite correct CAS UNII Ref fdacite correct FDA UNII 13AFD7670Q ChEMBL Ref ebicite correct EBI ChEMBL 856 KEGG Ref keggcite correct kegg KEGG D00474 InChI 1 C12H14N2O2 c1 2 12 9 6 4 3 5 7 9 10 15 13 8 14 11 12 16 h3 7H,2,8H2,1H3, H,13,15 H,14,16 InChIKey DQMZLTXERSFNPB UHFFFAOYAX smiles O C1NCNC O C1 c2ccccc2 CC StdInChI Ref stdinchicite correct chemspider StdInChI 1S C12H14N2O2 c1 2 12 9 6 4 3 5 7 9 10 15 13 8 14 11 12 16 h3 7H,2,8H2,1H3, H,13,15 H,14,16 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey DQMZLTXERSFNPB UHFFFAOYSA N CAS number Ref cascite correct ?? CAS number 125 33 7 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 4740 ATC prefix N03 ATC suffix AA03 ATC supplemental PubChem 4909 DrugBank Ref drugbankcite correct drugbank DrugBank DB00794 C 12 H 14 N 2 O 2 molecular weight 218.252 g mol bioavailability 100 ref name Ochoa 2005 cite web last Ochoa first Juan G coauthors Riche, Willise. year 2005 url http www.emedicine.com neuro topic692.htm title Antiepileptic Drugs An Overview work eMedicine publisher eMedicine, Inc. accessdate 2005 07 02 ref protein bound 25 ref name Ochoa 2005 metabolism Hepatic elimination half life Primidone 5 18 hours, br Phenobarbital 75 120 hours, ref name Ochoa 2005 br PEMA 16 hours ref name birf.info cite web author CDER, U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES year 2003 2005 title Primidone Mysoline work Pharmacology Guide for Brain Injury Treatment publisher Brain Injury Resource Foundation url http www.birf.info home bi tools qlinks anticon.html accessdate 2005 07 02 ref br Time to reach steady state br Primidone 2 3 days, br Phenobarbital&PEMA 1 4weeks ref name steadystate cite web author Yale Medical School, Department of Laboratory Medicine year 1998 title Therapeutic Drug Levels work YNHH Laboratory Manual Reference Documents publisher Yale Medical ... more details
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- List of dog diseases
causes of hemolytic lesion include hypophosphatemia , exposure to toxins such as lead , infections ... more details
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