autosomal dominant Kenny-Caffey syndrome (Q55950210)
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human disease
- Dwarfism, Cortical Thickening of Tubular Bones, and Transient Hypocalcemia
- Kenny-Caffey Syndrome Type 2
- Dwarfism, cortical thickening of tubular bones and transient hypocalcemia
- KCS2
- Kenny-Caffey syndrome, autosomal dominant
- KENNY-CAFFEY SYNDROME, TYPE 2
- KENNY-CAFFEY SYNDROME, TYPE 2; KCS2
- Kenny Syndrome
- Kenny-Caffey syndrome type 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant Kenny-Caffey syndrome |
human disease |
|
Statements
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C130993
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Identifiers
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