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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.370 Dysostoses .
C05.116.099.370.535 Klippel-Feil Syndrome .
C05.660 Musculoskeletal Abnormalities .
C05.660.551 Klippel-Feil Syndrome .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.077 Angiomatosis .
C14.907.077.410 Klippel-Trenaunay-Weber Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.551 Klippel-Feil Syndrome .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Klippel-Feil Syndrome .
Cervical Fusion Syndrome .
Klippel-Feil Sequence .
Vertebral Cervical Fusion Syndrome .
Dystrophia Brevicollis Congenitas .
Klippel Feil Syndrome .
Syndrome, Klippel-Feil .
Dystrophia Brevicollis Congenita .
A syndrome characterised by a low hairline and a shortened neck resulting from a reduced number of vertebrae or the fusion of multiple hemivertebrae into one osseous mass. .
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Klippel-Trenaunay-Weber Syndrome .
Angio-Osteohypertrophy Syndrome .
Angioosteohypertrophy Syndrome .
Congenital Dysplastic Angiopathy .
KTW Syndrome .
Klippel Trenaunay Syndrome .
Klippel-Trenaunay Syndrome .
Klippel-Trénaunay-Weber Syndrome .
Angio Osteohypertrophy Syndrome .
Angio-Osteohypertrophy Syndromes .
Angioosteohypertrophy Syndromes .
Angiopathies, Congenital Dysplastic .
Angiopathy, Congenital Dysplastic .
Congenital Dysplastic Angiopathies .
Disease, Klippel-Trenaunay .
Dysplastic Angiopathies, Congenital .
Dysplastic Angiopathy, Congenital .
KTW Syndromes .
Klippel Trenaunay Disease .
Klippel Trenaunay Weber Syndrome .
Klippel Trénaunay Weber Syndrome .
Klippel-Trenaunay Syndromes .
Syndrome, Angio-Osteohypertrophy .
Syndrome, Angioosteohypertrophy .
Syndrome, KTW .
Syndrome, Klippel Trenaunay .
Syndrome, Klippel-Trenaunay .
Syndrome, Klippel-Trenaunay-Weber .
Syndrome, Klippel-Trénaunay-Weber .
Syndromes, Angio-Osteohypertrophy .
Syndromes, Angioosteohypertrophy .
Syndromes, KTW .
Syndromes, Klippel-Trenaunay .
Klippel-Trenaunay Disease .
A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator. .
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