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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/257550
http://purl.bioontology.org/ontology/OMIM/257550
|
|---|---|
| Preferred Name | OCULAR MOTOR APRAXIA |
| Synonyms |
OCULOMOTOR APRAXIA, COGAN TYPE
COMA
SACCADE INITIATION FAILURE, CONGENITAL
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
OCULOMOTOR APRAXIA, COGAN TYPE
COMA
SACCADE INITIATION FAILURE, CONGENITAL
|
|---|---|
| prefLabel | OCULAR MOTOR APRAXIA
|
| Gene Symbol | COMA
|
| Scope Statement | Ocular movement dysfunction improves with age [MISCELLANEOUS]
|
| type | |
| Has manifestation | |
| tui | T047
|
| Gene Locus | 2q13
|
| MIMTYPEMEANING | Mendelian phenotype or locus, molecular basis unknown.
|
| notation | 257550
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C0543874
|
| OMIM Entry Type | 5
|
| OMIM MimType Value | perc
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |