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loading...| Preferred Name |
Visceral Myopathy 1 |
|
| Synonyms |
Visceral Myopathy 1 VSCM1 |
|
| Definitions |
An autosomal dominant type of functional intestinal obstruction caused by mutation(s) in the ACTG2 gene, encoding actin, gamma-enteric smooth muscle. |
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| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C201588 |
|
| code |
C201588 |
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| Concept_In_Subset | ||
| Contributing_Source |
Cellosaurus |
|
| DEFINITION |
An autosomal dominant type of functional intestinal obstruction caused by mutation(s) in the ACTG2 gene, encoding actin, gamma-enteric smooth muscle. |
|
| FULL_SYN |
Visceral Myopathy 1 VSCM1 |
|
| label |
Visceral Myopathy 1 |
|
| Preferred_Name |
Visceral Myopathy 1 |
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| prefixIRI |
Thesaurus:C201588 |
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| Semantic_Type |
Disease or Syndrome |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0020754 | EFO | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0020754 | MONDO | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/155310 | OMIM | LOOM |