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Osteogenesis Imperfecta:
"Autosomal dominant COLLAGEN DISEASES resulting from defective biosynthesis of COLLAGEN TYPE I and characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. There are four major types, I-IV."
Ατελής Οστεογένεση:
"Αυτοχρωμοσωματική επικρατούσα ΑΣΘΕΝΕΙΑ ΤΟΥ ΚΟΛΛΑΓΟΝΟΥ ως αποτέλεσμα της ελαττωματικής βιοσύνθεσης του ΚΟΛΛΑΓΟΝΟΥ ΤΥΠΟΥ Ι (COLLAGEN TYPE I) η οποία χαρακτηρίζεται από εύθραυστα, οστεοπορωτικά οστά τα οποία παθαίνουν εύκολα κατάγματα. Μπορεί επίσης να συνυπάρχουν μπλε σκληρός, χαλαρές αρθρώσεις και ατελής σχηματισμό της οδοντίνης. Υπάρχουν τέσσερις βασικοί τύποι, I-IV."
Source: Medical Subject Headings, 2005_2005_01_17

 

Synonym / term
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Code
 
Source vocabulary
 
UMLS Concept Unique Identifier
 
osteogenesis imperfecta 1849-7175 CRISP Thesaurus, 2004 C0029434
brittle bone disease 1849-7175 CRISP Thesaurus, 2004 C0029434
Osteogenesis imperfecta 756.51 ICD-9-CM, 2005 C0029434
Osteopsathyrosis 756.51 Metathesaurus additional entry terms for ICD-9-CM, 2005, 2005 C0029434
Fragilitas ossium 756.51 Metathesaurus additional entry terms for ICD-9-CM, 2005, 2005 C0029434
Osteogenesis Imperfecta C26837 NCI Thesaurus, 2004_11_17 C0029434
Osteogenesis Imperfecta C4602 National Drug File - Reference Terminology, 2004_01 C0029434
Fragilitas Ossium D010013 Medical Subject Headings, 2005_2005_01_17 C0029434
Osteogenesis Imperfecta D010013 Medical Subject Headings, 2005_2005_01_17 C0029434
Ossiums, Fragilitas D010013 Medical Subject Headings, 2005_2005_01_17 C0029434
OSTEOPSATHYROSIS NOCODE DXplain, 1994 C0029434
Osteogenesis Imperfecta NOCODE COSTAR, 1989-1995 C0029434
Osteogenesis imperfecta Q78.0 German translation of ICD10, 1995 C0029434
Osteogenesis Imperfecta T940 MedlinePlus Health Topics_2004_08_14, 20040814 C0029434
OSTEOGENESIS IMPERFECTA U001348 DXplain, 1994 C0029434
Osteopsathyrosis U005900 Library of Congress Subject Headings, 1990 C0029434
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