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loading...| Preferred Name |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
| ID |
http://purl.bioontology.org/ontology/MESH/C563529 |
| cui |
C1834339 |
| HM |
D017696 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20121105 |
| MeSH Frequency |
0 |
| notation |
C563529 |
| prefLabel |
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
| SC |
3 |
| Scope Statement |
PROM mutation in ACTA1 |
| TERMUI |
T827924 |
| TH |
OMIM (2013) |
| tui |
T047 |
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| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/161800 | Online Mendelian Inheritance in Man | CUI | |
| http://purl.bioontology.org/ontology/OMIM/102610 | Online Mendelian Inheritance in Man | CUI |