Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) RatMine GViewer (Genome Viewer) Overgo Probe Designer ACP Haplotyper Genome Scanner
Aging & Age-Related Disease Cancer Cardiovascular Disease COVID-19 Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
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
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Poster Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

Ontology Browser
Term:
Lissencephaly 9 with Complex Brainstem Malformation (DOID:9005346)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
lissencephaly +     
Baraitser-Winter syndrome +   
Classical Lissencephalies and Subcortical Band Heterotopias +   
Cobblestone Lissencephaly +   
Familial Lissencephaly with Cleft Palate and Cerebellar Hypoplasia 
Frontotemporal Pachygyria 
Lissencephaly 10  
Lissencephaly 3 +   
Lissencephaly 4  
Lissencephaly 5  
Lissencephaly 6, with Microcephaly  
Lissencephaly 7 with Cerebellar Hypoplasia  
Lissencephaly 8  
Lissencephaly 9 with Complex Brainstem Malformation  
An autosomal dominant neurologic disorder characterized by global developmental delay apparent since infancy, impaired intellectual development with poor or absent speech.
Massa Casaer Ceulemans Syndrome 
Mental Retardation, Autosomal Recessive 34, with variant lissencephaly  
Miller-Dieker lissencephaly syndrome  
Norman-Roberts syndrome  
Pachygyria with Mental Retardation, Seizures, and Arachnoid Cysts 
PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES  
Partial Lissencephaly 
Winter Harding Hyde Syndrome 

Synonyms
Exact Synonyms: LIS9 ;   SPECTRAPLAKINOPATHY TYPE I ;   lissencephaly 9 ;   lissencephaly with decussation defect
Primary IDs: OMIM:618325

paths to the root