serw-MX  [xml]  
 


    
 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 .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.551 Klippel-Feil Syndrome .
G02 Chemical Phenomena .
G02.111 Biochemical Phenomena .
G02.111.570 Molecular Structure .
G02.111.570.080 Base Sequence .
G05 Genetic Phenomena .
G05.360 Genetic Structures .
G05.360.080 Base Sequence .
L01 Information Science .
L01.453 Information Services .
L01.453.245 Documentation .
L01.453.245.667 Molecular Sequence Data .
L01.453.245.667.080 Base Sequence .
SP8 Disasters .
SP8.946 Disaster Management .
SP8.946.819 Prevention and Mitigation .
SP8.946.819.964 Simulacra .
 
 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. .
1.00
 
Simulacra .
Simulacrum .
Feint .
0.45
 
Base Sequence .
DNA Sequences .
Base Sequences .
Nucleotide Sequences .
RNA Sequences .
Sequence, Base .
Sequence, DNA .
Sequence, Nucleotide .
Sequence, RNA .
Sequences, Base .
Sequences, DNA .
Sequences, Nucleotide .
Sequences, RNA .
Nucleotide Sequence .
RNA Sequence .
DNA Sequence .
NUCLEOSIDE SEQUENCE .
TRANSFORMING REGION .
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence. .
0.41