congenital muscular dystrophy due to integrin alpha-7 deficiency (Q32139695)
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congenital muscular dystrophy characterized by autosomal recessive inheritance that has material basis in compound heterozygous mutation in the ITGA7 gene on chromosome 12q13
- congenital muscular dystrophy with integrin alpha-7 deficiency
- congenital myopathy due to integrin alpha-7 deficiency
- congenital muscular dystrophy with ITGA7 deficiency
- MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY
- Myopathy, Congenital, Due to Integrin Alpha-7 Deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital muscular dystrophy due to integrin alpha-7 deficiency |
congenital muscular dystrophy characterized by autosomal recessive inheritance that has material basis in compound heterozygous mutation in the ITGA7 gene on chromosome 12q13 |
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