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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

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