Hypotelorism - cleft palate - hypospadias (Q94180): Difference between revisions
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Síndrome de Schilbach-Rott, ou síndrome de hipotelorismo - fenda palatina - hipospádia é caracterizada por fenda palatina e hipotelorismo ocular. | |||
| description / en | description / en | ||
Schilbach-Rott syndrome, or hypotelorism - cleft palate - hypospadias syndrome is characterised by cleft palate and ocular hypotelorism. | |||
Revision as of 09:18, 16 August 2026
Schilbach-Rott syndrome, or hypotelorism - cleft palate - hypospadias syndrome is characterised by cleft palate and ocular hypotelorism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1481992489 |
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| English | Hypotelorism - cleft palate - hypospadias |
Schilbach-Rott syndrome, or hypotelorism - cleft palate - hypospadias syndrome is characterised by cleft palate and ocular hypotelorism. |
