WormBase Tree Display for DO_term: DOID:0110936
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| DOID:0110936 | Name | nemaline myopathy 5A | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A nemaline myopathy that has_material_basis_in autosomal recessive inheritance of a homozygous mutation in the TNNT1 gene on chromosome 19q13, with infantile onset. | ||||
| Synonym | Exact | ANM | |||
| Amish nemaline myopathy | |||||
| NEM5 | |||||
| nemaline myopathy 5, Amish type | |||||
| Parent | Is_a | DOID:3191 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 605355 | |
| Attribute_of | Gene_by_orthology | WBGene00003495 | |||
| WBGene00006587 | |||||
| WBGene00006588 | |||||
| WBGene00006589 |
