Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Modify Subscription
Unsubscribe
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Modify Subscription
Unsubscribe
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
{{ loginError }}
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be sent 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
Variants
Community Projects
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
OntoMate (Literature Search)
JBrowse (Genome Browser)
Synteny Browser (VCMap)
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)
Diseases
Aging & Age-Related Disease
Cancer & Neoplastic Disease
Cardiovascular Disease
Coronavirus Disease
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
Genetic Models
Autism Models
Rat PhenoMiner (Quantitative Phenotypes)
Chinchilla PhenoMiner
Expected Ranges (Quantitative Phenotype)
PhenoMiner Term Comparison
Hybrid Rat Diversity Panel
Phenotypes
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 Presentations Archive
Nomenclature Guidelines
Resource Links
Laboratory Resources
Employment Resources
Advanced Search (OLGA)
Ontology Browser
Term:
skeletal system disease
(EFO:0002461)
Annotations:
Rat: (0)
Mouse: (0)
Human: (10170)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Naked Mole-rat: (0)
Green Monkey: (0)
Parent Terms
Term With Siblings
Child Terms
musculoskeletal system disease
+
auriculoosteodysplasia
autoimmune disorder of musculoskeletal system
+
chondrodysplasia with joint dislocations, gPAPP type
CINCA syndrome
+
enthesopathy
+
Klippel-Feil syndrome
+
ligament disorder
+
muscle tissue disorder
+
muscular disease
+
musculoskeletal system benign neoplasm
+
musculoskeletal system cancer
+
musculoskeletal toxicity
osteoglophonic dwarfism
osteoporosis-oculocutaneous hypopigmentation syndrome
Ramon syndrome
short stature, Brussels type
Short stature, Dauber-Argente type
skeletal system disease
+
A disease involving the skeletal system. Any disease which affects part of the skeletal system.
Synovial Chondromatosis
synovium disorder
+
Upington disease
wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia
Adamantinomatous Craniopharyngioma
Al-Gazali syndrome
bone disease
+
bone marrow disorder
+
brachydactyly
+
brachydactyly-syndactyly syndrome
brachydactyly-syndactyly-oligodactyly syndrome
Brachymorphism-onychodysplasia-dysphalangism syndrome
Buschke-Ollendorff syndrome
cartilage disease
+
cartilage-hair hypoplasia
+
cervical spondylosis
cherubism
chondroma
+
Coffin-Siris syndrome
+
endocrine-cerebro-osteodysplasia syndrome
fibrodysplasia ossificans progressiva
flatfoot
Hammer Toe Syndrome
joint disease
+
Marfan syndrome
+
metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
microcephaly-brachydactyly-kyphoscoliosis syndrome
multiple congenital anomalies-hypotonia-seizures syndrome 3
ossification of the posterior longitudinal ligament of the spine
Papillary Craniopharyngioma
polydactyly
+
primary basilar invagination
Pubic Symphysis Diastasis
Rare genetic bone development disorder
+
rheumatic disease
+
Rienhoff syndrome
scalp defects-postaxial polydactyly syndrome
short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis
short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
symphalangism
+
syndactyly
+
Synovial Chondromatosis
Teebi-Shaltout syndrome
temtamy preaxial brachydactyly syndrome
tooth disease
+
vertebral column disorder
+
Synonyms
Exact Synonyms:
disease of skeletal system ; disease or disorder of skeletal system ; disorder of skeletal system ; skeletal system disease or disorder ; skeletal system disorder
Related Synonyms:
disease of bone and/or joint ; osteoarthropathy
Xrefs:
ICD10:M43 ; MEDGEN:538042 ;
MONDO:0005172
; SCTID:88230002 ; UMLS:C0263661
External Ontologys:
disease_has_location EFO:UBERON:0001434
Definition Sources:
https://orcid.org/0000-0002-6601-2165