Ontology Browser

Term:
Oculomotor Apraxia, Cogan Type (DOID:9007586)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2)
Parent Terms Term With Siblings Child Terms
apraxia +     
Cogan syndrome +     
Alien Hand Syndrome 
Alzheimer's Disease, Familial, 3, with Spastic Paraparesis and Apraxia  
ataxia with oculomotor apraxia type 1  
ataxia with oculomotor apraxia type 3  
Ataxia-Oculomotor Apraxia 4  
epithelial basement membrane dystrophy  
gait apraxia 
ideomotor apraxia 
Miles-Carpenter syndrome  
Oculomotor Apraxia, Cogan Type  
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant  
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked  
Specific Language Impairment 4 
Speech-Language Disorder 1  

Synonyms
Exact Synonyms: COMA ;   Cogan's syndrome, type 2 ;   Ocular Motor Apraxia ;   congenital oculomotor apraxia ;   congenital saccade initiation failure
Primary IDs: MESH:C537423
Alternate IDs: OMIM:257550 ;   RDO:0003267

paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.