ONKI3 | Medical Subject Headings

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The way concept relations are shown: separately in hierarchy

Klippel-Feil Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Musculoskeletal Abnormalities ∟ Klippel-Feil Syndrome 12 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hajdu-Cheney Syndrome \| ∟ Hip Dislocation, Congenital \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Craniofacial Dysostosis \| ∟ Focal Dermal Hypoplasia \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dysostoses ∟ Klippel-Feil Syndrome 12 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hajdu-Cheney Syndrome \| ∟ Hip Dislocation, Congenital \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Craniofacial Dysostosis \| ∟ Focal Dermal Hypoplasia \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Musculoskeletal Abnormalities ∟ Klippel-Feil Syndrome 12 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hajdu-Cheney Syndrome \| ∟ Hip Dislocation, Congenital \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Craniofacial Dysostosis \| ∟ Focal Dermal Hypoplasia \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Musculoskeletal Abnormalities ∟ Klippel-Feil Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dysostoses ∟ Klippel-Feil Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Musculoskeletal Abnormalities ∟ Klippel-Feil Syndrome Musculoskeletal Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Dysostoses > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Musculoskeletal Abnormalities > Musculoskeletal Diseases > Medical Subject Headings (MeSH) X
Annotation:	short neck as result of vertebral abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
Scope note:	A condition characterized by shortness of the neck resulting from reduction in the number of vertebrae or the fusion of multiple hemivertebrae into one osseous mass. The hairline is low and the motion of the neck is limited. (Dorland, 27th ed) X
activeMeSHYear*:	2000 \| 2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	1999-11-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	kleX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Arthrogryposis \| Craniofacial Abnormalities \| Funnel Chest \| Gastroschisis \| Hajdu-Cheney Syndrome \| Hip Dislocation, Congenital \| Limb Deformities, Congenital \| Synostosis \| Craniofacial Dysostosis \| Focal Dermal Hypoplasia \| Orofaciodigital Syndromes \| Rubinstein-Taybi Syndrome X
URI:	X
Labels and equivalent concepts:	Klippel-Feilin oireyhtymä (fi) Klippel-Feilin syndrooma (fi, replaced) Kaularangan fuusio-syndrooma (fi, replaced) Kaularangan fuusio (fi, replaced) Kaularangan fuusio-oireyhtymä (fi, replaced) Klippel-Feils syndrom (sv) Dystrophia Brevicollis Congenita (en, replaced) Syndroma fusionis cervicalis (la-FI, replaced) Syndroma Klippel-Feil (la-FI, replaced) X
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