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Ontology Browser

Term:
Periventricular Nodular Heterotopia 9 (DOID:9001401)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Periventricular Laminar Heterotopia 
Periventricular Nodular Heterotopia 2  
Periventricular Nodular Heterotopia 3 
Periventricular Nodular Heterotopia 4  
Periventricular Nodular Heterotopia 5 
Periventricular Nodular Heterotopia 6  
Periventricular Nodular Heterotopia 7  
Periventricular Nodular Heterotopia 8  
Periventricular Nodular Heterotopia 9  
An autosomal dominant neurologic disorder characterized as a malformation of cortical development caused by heterozygous mutation in the MAP1B gene on chromosome 5q13. (OMIM)
Periventricular Nodular Heterotopia, with Frontometaphyseal Dysplasia 

Synonyms
Exact Synonyms: PVNH9
Primary IDs: OMIM:618918

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