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:
congenital nervous system abnormality
(DOID:2490)
Annotations:
Rat: (1536)
Mouse: (1545)
Human: (2029)
Chinchilla: (1466)
Bonobo: (1535)
Dog: (1532)
Squirrel: (1493)
Pig: (1520)
Naked Mole-rat: (1448)
Green Monkey: (1515)
Parent Terms
Term With Siblings
Child Terms
nervous system disease
+
physical disorder
+
agnathia-otocephaly complex
alpha-methylacyl-CoA racemase deficiency
arthrogryposis multiplex congenita
+
autoimmune disease of the nervous system
+
autonomic nervous system disease
+
autosomal dominant congenital deafness with onychodystrophy
autosomal recessive congenital ichthyosis
+
BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME
bladder exstrophy-epispadias-cloacal exstrophy complex
+
blepharophimosis
+
caudal regression syndrome
central nervous system disease
+
Chronobiology Disorders
+
cleft palate-lateral synechia syndrome
Compton-North congenital myopathy
congenital adrenal hyperplasia
+
congenital adrenal insufficiency
congenital afibrinogenemia
+
congenital amegakaryocytic thrombocytopenia
+
congenital aphakia
congenital bilateral absence of vas deferens
+
congenital bile acid synthesis defect
+
Congenital Cataracts, Facial Dysmorphism, and Neuropathy
congenital central hypoventilation syndrome
+
congenital chylothorax
congenital contractural arachnodactyly
congenital diaphragmatic hernia
+
congenital diarrhea
+
congenital disorder of glycosylation
+
congenital epulis
congenital fibrosarcoma
congenital fibrosis of the extraocular muscles
+
Congenital Foot Deformities
+
congenital generalized lipodystrophy
+
congenital granular cell tumor
congenital heart block
+
congenital heart disease
+
congenital hemolytic anemia
+
congenital hereditary endothelial dystrophy of cornea
congenital hypogammaglobulinemia
congenital hypoplastic anemia
+
congenital hypothyroidism
+
congenital hypotrichosis with juvenile macular dystrophy
congenital intrinsic factor deficiency
congenital lactase deficiency
congenital leptin deficiency
congenital megabladder
congenital mesoblastic nephroma
+
congenital mirror movement disorder
+
congenital muscular dystrophy
+
congenital myasthenic syndrome
+
congenital myopathy 4A
+
congenital nervous system abnormality
+
congenital nystagmus
+
congenital ptosis
+
congenital stationary night blindness
+
congenital stromal corneal dystrophy
congenital structural myopathy
+
congenital sucrase-isomaltase deficiency
congenital syphilis
+
congenital toxoplasmosis
cryptophthalmia
+
diplegia of upper limb
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
gastroschisis
+
Gerstmann syndrome
herpes zoster
+
hypospadias
+
imperforate anus
+
Infantile Multisystem Neurologic Disease with Osseous Fragility
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease
+
intestinal pseudo-obstruction
+
Klippel-Feil syndrome
+
large congenital melanocytic nevus
laryngomalacia
+
Leber congenital amaurosis
+
lethal congenital contracture syndrome
+
lethal congenital glycogen storage disease of heart
LETM1-ASSOCIATED CLINICAL SPECTRUM WITH PREDOMINANT NERVOUS SYSTEM INVOLVEMENT
Meckel's diverticulum
MLS syndrome
+
multiple congenital anomalies-hypotonia-seizures syndrome
+
myotonia congenita
+
Nerve Injuries
+
Nervous System Malformations
+
Nervous System Neoplasms
+
Nervous System Trauma
+
neural tube defect
+
Neurocutaneous Syndromes
+
neurodegenerative disease
+
Neurologic Manifestations
+
non-congenital cyst of kidney
nonsyndromic congenital nail disorder
+
Norrie disease
omphalocele
orofacial cleft
+
palmoplantar keratoderma and congenital alopecia 1
palmoplantar keratoderma and congenital alopecia 2
peripheral nervous system disease
+
Poland syndrome
polydactyly
+
Polyglucosan Body Disease, Adult Form
primary congenital glaucoma
+
radioulnar synostosis
+
rapidly involuting congenital hemangioma
Roy Maroteaux Kremp Syndrome
sensory system disease
+
severe congenital encephalopathy due to MECP2 mutation
severe congenital neutropenia
+
Silver-Russell syndrome
+
spondyloepiphyseal dysplasia with congenital joint dislocations
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
Tang Hsi Ryu Syndrome
TORCH syndrome
toxic encephalopathy
+
visceral heterotaxy
+
Zika virus congenital syndrome
anencephaly
+
ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES
holoprosencephaly
+
lissencephaly
+
microcephaly
+
Periventricular Laminar Heterotopia
periventricular nodular heterotopia
+
tubulinopathy
Synonyms
Exact Synonyms:
congenital neurologic anomaly
Xrefs:
ICD9CM:742
Definition Sources:
MESH:D020763