Perrault syndrome (Q18553517)
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autosomal recessive disesase that is characterized by sensorineural hearing loss and ovarian failure
- PRLTS1
- Ovarian Dysgenesis With Sensorineural Deafness
- PERRAULT SYNDROME 1
- Gonadal Dysgenesis, 20 Type, With Deafness
- Perrault Syndrome type 1
- PERRAULT SYNDROME 1; PRLTS1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Perrault syndrome |
autosomal recessive disesase that is characterized by sensorineural hearing loss and ovarian failure |
|
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Sitelinks
Wikipedia(2 entries)
- dewiki Perrault-Syndrom
- ruwiki Синдром Перро