×
Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Update Watcher
Remove Watcher
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Update Watcher
Remove Watcher
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
×
Save what matters to you
{{ loginError }}
Sign in with your RGD account
Email Address:
Password:
Create New Account
Recover Password
×
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be send to {{ username }}
{{geneWatchAttr}}
Analyze
Gene
Strain
QTL
List
×
Gene Annotator (Functional Annotation)
unavailable
Gene Annotator (Annotation Distribution)
unavailable
Variant Visualizer (Genomic Variants)
unavailble
Variant Visualizer (Genomic Variants)
unavailable
Gene Annotator (Functional Annotation)
Gene Annotator (Annotation Distribution)
Variant Visualizer (Genomic Variants)
InterViewer (Protein-Protein Interactions)
unavailable
Gviewer (Genome Viewer)
unavailable
Variant Visualizer (Damaging Variants) unavailble
Variant Visualizer (Damaging Variants)
unavailable
InterViewer (Protein-Protein Interactions)
GViewer (Genome Viewer)
Variant Visualizer (Damaging Variants)
Gene Annotator (Annotation Comparison)
unavailable
OLGA (Gene List Generator)
unavailable
Gene Annotator (Annotation Comparison)
OLGA (Gene List Generator)
Excel (Download)
MOET (Multi-Ontology Enrichement)
unavailable
GOLF (Gene-Ortholog Location Finder)
unavailable
MOET (Multi-Ontology Enrichement)
GOLF (Gene-Ortholog Location Finder)
x
Send Message
x
Send us a Message
Your email
Message
Send
Submit Data
|
Help
|
Video Tutorials
|
News
|
Publications
|
Download
|
REST API
|
Citing RGD
|
Contact
Home
Search RGD
Grant Resources
Citing RGD
About Us
Contact Us
Data
Genes
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
OntoMate (Literature Search)
JBrowse (Genome Browser)
Synteny Browser (VCMap)
(beta)
Variant Visualizer
Multi-Ontology Enrichment (MOET)
Gene-Ortholog Location Finder (GOLF)
InterViewer (Protein-Protein Interactions)
PhenoMiner (Quatitative Phenotypes)
Gene Annotator
OLGA (Gene List Generator)
AllianceMine
GViewer (Genome Viewer)
Overgo Probe Designer
Diseases
Aging & Age-Related Disease
Cancer & Neoplastic Disease
Cardiovascular Disease
COVID-19
Developmental Disease
Diabetes
Hematologic Disease
Immune & Inflammatory Disease
Infectious Disease
Liver Disease
Neurological Disease
Obesity & Metabolic Syndrome
Renal Disease
Respiratory Disease
Sensory Organ Disease
Phenotypes & Models
Find Models
new
Genetic Models
Autism Models
PhenoMiner (Quantitative Phenotypes)
Expected Ranges (Quantitative Phenotype)
PhenoMiner Term Comparison
Hybrid Rat Diversity Panel
Phenotypes
GERRC (Gene Editing Rat Resource Center)
Phenotypes in Other Animal Models
Animal Husbandry
Strain Medical Records
Phylogenetics
Strain Availability
Calendar
Rats 101
Submissions
Photo Archive
Pathways
Community
Rat Community Forum
Directory of Rat Laboratories
Video Tutorials
News
RGD Publications
RGD Poster Archive
Nomenclature Guidelines
Resource Links
Laboratory Resources
Employment Resources
Advanced Search (OLGA)
Ontology Browser
Term:
scoliosis
(DOID:0060249)
Annotations:
Rat: (64)
Mouse: (65)
Human: (71)
Chinchilla: (62)
Bonobo: (64)
Dog: (64)
Squirrel: (63)
Pig: (64)
Parent Terms
Term With Siblings
Child Terms
bone structure disease
+
Spinal Curvatures
+
bone deterioration disease
+
Camptocormia
Kyphosis
+
Lordosis
+
scoliosis
+
A bone structure disease characterized by an appreciable lateral deviation in the normally straight vertical line of the spine. (DO)
Spinal Curvatures
+
spondylolisthesis
+
spondylolysis
+
spondylosis
+
Acrodysplasia Scoliosis
CEREBELLAR DYSFUNCTION, IMPAIRED INTELLECTUAL DEVELOPMENT, AND HYPOGONADOTROPIC HYPOGONADISM
Cervical Hypertrichosis with Underlying Kyphoscoliosis
Coffin Syndrome 1
Congenital Myopathy 19
Daish Hardman Lamont Syndrome
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation
Familial Horizontal Gaze Palsy with Progressive Scoliosis
+
idiopathic scoliosis
Iida Kannari Syndrome
Kyphoscoliosis
+
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis
Omphalocele Exstrophy Imperforate Anus
parastremmatic dwarfism
Pilotto Syndrome
Prata Libéral Gonçalves Syndrome
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa
rigid spine muscular dystrophy 1
Scoliosis, Arachnodactyly, and Blindness
SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME
Short Stature, Amelogenesis Imperfecta, and Skeletal Dysplasia with Scoliosis
Shprintzen Omphalocele Syndrome
spondylocarpotarsal synostosis syndrome
Tsukahara Syndrome
Waaler Aarskog Syndrome
Synonyms
Exact Synonyms:
scolioses
Narrow Synonyms:
congenital scoliosis
Primary IDs:
MESH:D012600
Xrefs:
EFO:0004273
;
ICD10CM:M41.9
;
MONDO:0005392
;
NCI:C78603
Definition Sources:
http://en.wikipedia.org/wiki/Scoliosis
"DO" "DO",
http://www.mayoclinic.org/diseases-conditions/scoliosis/basics/definition/con-20030140
"DO" "DO"