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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/157600
http://purl.bioontology.org/ontology/OMIM/157600
|
|---|---|
| Preferred Name | MIRROR MOVEMENTS 1 |
| Synonyms |
BIMANUAL SYNERGIA
MRMV1
MIRROR MOVEMENTS 1 AND/OR AGENESIS OF THE CORPUS CALLOSUM
MIRROR MOVEMENTS, CONGENITAL
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
BIMANUAL SYNERGIA
MRMV1
MIRROR MOVEMENTS 1 AND/OR AGENESIS OF THE CORPUS CALLOSUM
MIRROR MOVEMENTS, CONGENITAL
|
|---|---|
| prefLabel | MIRROR MOVEMENTS 1
|
| Gene Symbol |
DCC
HGPPS2
MRMV1
|
| Scope Statement | Caused by mutation in the deleted in colorectal carcinoma gene (DCC, 120470.0001) [MOLECULAR BASIS]
Disorder usually remains stable over time [MISCELLANEOUS]
Onset in infancy or early childhood [MISCELLANEOUS]
Incomplete penetrance [MISCELLANEOUS]
Highly variable phenotype [MISCELLANEOUS]
|
| type | |
| Has manifestation |
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|
| tui | T033
|
| Gene Locus | 18q21.3
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| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 157600
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1834870
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
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| No notes to display |