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Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Perrault syndrome
Summary
- Definition
- A syndrome that is characterized by sensorineural hearing loss and ovarian failure.
- Super Class
- autosomal recessive disease syndrome
External Links
- Disease Ontology
- DOID:0050857
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001272 | Cerebellar atrophy |
| HP:0000218 | High palate |
| HP:0002066 | Gait ataxia |
| HP:0001260 | Dysarthria |
