About: Connective Tissue Disorder

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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Connective Tissue Disorder
rdfs:subClassOf	Connective and Soft Tissue Disorder nodeID://b661453
Has_CDRH_Parent	Patient Problem
Has_NICHD_Parent	Disease
Concept_In_Subset	Patient Problem Codes FDA CDRH NICHD Terminology Neonatal Research Network Terminology
Semantic_Type	Disease or Syndrome
Preferred_Name	Connective Tissue Disorder
UMLS_CUI	C0009782
FDA_Table	Patient Code (Appendix B)
Contributing_Source	FDA NICHD
ALT_DEFINITION	A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides.MSH2003_2003_05_12
Legacy_Concept_Name	Connective_Tissue_Disorder
FULL_SYN	Connective Tissue DiseaseSYNCI Connective Tissue DiseasesSYNCI Connective Tissue DisorderPTNCI Connective Tissue DisordersSYNCI Connective Tissue DisorderPTNICHD CONNECTIVE TISSUE DISEASEPTFDA1786 Disorder of Connective TissueSYNICHD DISEASE, CONNECTIVE TISSUESYFDA1786 TISSUE DISEASE, CONNECTIVESYFDA1786
DEFINITION	A congenital or acquired disorder characterized by abnormalities in one or more of the elements of the connective tissues.NCI
code	C26729
http://linked.open...y/mesh/hasConcept	http://linked.opendata.cz/resource/mesh/concept/M0005027
is rdf:first of	nodeID://b738906 nodeID://b738907
is rdfs:subClassOf of	Interstitial Disease Non-Neoplastic Bone Disorder Hereditary Connective Tissue Disorder
is Has_NICHD_Parent of	Hereditary Connective Tissue Disorder
is sameAs of	Connective Tissue Diseases

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