Klippel-Feil Syndrome [Klippelův-Feilův syndrom]
- Terms
-
Cervical Fusion Syndrome
Dystrophia Brevicollis Congenita
Klippel-Feil Sequence
Vertebral Cervical Fusion Syndrome
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.
- Annotation
- short neck as result of vertebral abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
- DUI
- D007714 MeSH Browser
- CUI
- M0012063
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications 1
- DI
- diagnosis 2
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 2
- GE
- genetics 2
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery 1
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology
Calabro syndrome Disease MeSH Browser
Klippel Feil syndrome dominant type Disease MeSH Browser
Klippel Feil syndrome recessive type Disease MeSH Browser
Segmentation syndrome 1 Disease MeSH Browser