WormBase Tree Display for DO_term: DOID:0110931
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| DOID:0110931 | Name | nemaline myopathy 10 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A nemaline myopathy characterized by early-onset generalized muscle weakness and hypotonia with respiratory insufficiency and feeding difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD3 gene on chromosome 3p14. | ||||
| Synonym | Exact | NEM10 | |||
| congenital myopathy 10 | |||||
| Parent | Is_a | DOID:3191 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 616165 | |
| Attribute_of | Gene_by_orthology | WBGene00006823 |
