You are using an outdated browser. Please upgrade your browser to improve your experience.
Perrault syndrome 4
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any Perrault syndrome in which the cause of the disease is a mutation in the LARS2 gene.
Uniprot Description An autosomal recessive, sex-influenced disorder characterized by sensorineural deafness in both males and females, and ovarian dysgenesis in females. Affected females have primary amenorrhea, streak gonads, and infertility, whereas affected males show normal pubertal development and are fertile.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:615300
UMLS:C3809105
MONDO:0014126
High level summary of knowledge for a disease, including descriptions and datasource references.