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loading...| Preferred Name |
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency |
| ID |
http://purl.bioontology.org/ontology/MESH/C564317 |
| cui |
C1842898 |
| Has mapping qualifier | |
| HM |
D009136/Q000151 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20121105 |
| MeSH Frequency |
1 |
| MMR |
20131106 |
| notation |
C564317 |
| prefLabel |
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency |
| SC |
3 |
| Scope Statement |
mutation in laminin alpha-2 (LAMA2) |
| TERMUI |
T829440 |
| TH |
OMIM (2013) |
| tui |
T047 |