WormBase Tree Display for DO_term: DOID:0110639
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| DOID:0110639 | Name | congenital muscular dystrophy due to integrin alpha-7 deficiency | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A congenital muscular dystrophy characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the ITGA7 gene on chromosome 12q13. | ||||
| Synonym | Exact | congenital muscular dystrophy with ITGA7 deficiency | |||
| congenital muscular dystrophy with integrin alpha-7 deficiency | |||||
| congenital myopathy due to integrin alpha-7 deficiency | |||||
| Parent | Is_a | DOID:0050557 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 613204 | |
| Attribute_of | Gene_by_orthology | WBGene00002081 |
