2p21 microdeletion syndrome (Q56013735)
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The 2p21 microdeletion syndrome consists of cystinuria, neonatal seizures, hypotonia, severe growthand developmental delay, facial dysmorphism, and lactic acidemia
- Monosomy 2p21
- 2p21 deletion syndrome
- Del(2)(p21)
- 2p21 deletion
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 2p21 microdeletion syndrome |
The 2p21 microdeletion syndrome consists of cystinuria, neonatal seizures, hypotonia, severe growthand developmental delay, facial dysmorphism, and lactic acidemia |
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1 reference
1 reference
1 reference