ocular motor apraxia |
Disease ID | 1710 |
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Disease | ocular motor apraxia |
Definition | Ocular motor apraxia is a deficiency in voluntary, horizontal, lateral, fast eye movements (saccades) with retention of slow pursuit movements. The inability to follow objects visually is often compensated by head movements. There may be decreased smooth pursuit, and cancellation of the vestibulo-ocular reflex. [HPO:probinson, pmid:20615230] |
Synonym | apraxia, oculomotor, cogan type cogan's syndrome, type 2 congenital oculomotor apraxia oculomotor apraxia - cogan type oculomotor apraxia - cogan type (disorder) oculomotor apraxia, cogan type saccade initiation failure, congenital |
OMIM | |
UMLS | C0543874 |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:2) |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | (Waiting for update.) |
Locus | (Waiting for update.) |
Disease ID | 1710 |
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Disease | ocular motor apraxia |
Integrated Phenotype | HPO | Name(Total Integrated Phenotypes:3) HP:0008026 | Horizontal opticokinetic nystagmus HP:0000657 | Oculomotor apraxia HP:0006961 | Jerking head movements |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:4) HP:0001251 | Ataxia | 5 HP:0002073 | Cerebellar ataxia, progressive | 2 HP:0000556 | Retinal dystrophy | 1 HP:0001009 | Telangiectases | 1 |
Disease ID | 1710 |
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Disease | ocular motor apraxia |
Manually Symptom | (Waiting for update.) |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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Mapped by lexical matching(Total Items:0) |
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Mapped by homologous gene(Total Items:0) |
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Chemical(Total Drugs:0) | |
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