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Perrault syndrome 2

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any Perrault syndrome in which the cause of the disease is a mutation in the HARS2 gene.
Uniprot Description A 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.
Mondo Term and Equivalent IDs
MONDO:0013972:  Perrault syndrome 2
UMLS:C3554105: