WormBase Tree Display for DO_term: DOID:0110640
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| DOID:0110640 | Name | congenital muscular dystrophy due to LMNA mutation | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A congenital muscular dystrophy characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the LMNA gene on chromosome 1q22. | ||||
| Synonym | Exact | L-CMD | |||
| LMNA-related congenital muscular dystrophy | |||||
| congenital muscular dystrophy LMNA-related | |||||
| Parent | Is_a | DOID:0050557 | |||
| DOID:0050736 | |||||
| DB_info | Database | OMIM | disease | 613205 | |
| Attribute_of | Gene_by_orthology | WBGene00003052 |
