SADDAN (Q259765)
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autosomal dominant disease characterized by severe achondroplasia, developmental delay and acanthosis nigricans that has material basis in heterozygous mutation in the FGFR3 gene on chromosome 4p16
- Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans
- severe achondroplasia with developmental delay and acanthosis nigricans
- ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN
- SADDAN dysplasia
- ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | SADDAN |
autosomal dominant disease characterized by severe achondroplasia, developmental delay and acanthosis nigricans that has material basis in heterozygous mutation in the FGFR3 gene on chromosome 4p16 |
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Statements
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757.39
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783.40
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Identifiers
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Sitelinks
Wikipedia(5 entries)
- bswiki SADDAN
- dewiki SADDAN-Dysplasie
- enwiki Severe achondroplasia with developmental delay and acanthosis nigricans
- frwiki SADDAN
- huwiki SADDAN-szindróma