autosomal dominant chondrodysplasia punctata (Q18649173)
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Human disease
- Chondrodysplasia punctata, Sheffield type
- chondrodysplasia punctata, autosomal dominant
- Chondrodysplasia Punctata Due to Vitamin K Deficiency
- Chondrodysplasia Punctata Due to Warfarin Teratogenicity
- chondrodysplasia punctata Sheffield type
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant chondrodysplasia punctata |
Human disease |
|
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