ORPHA:642945
Perrault syndrome type 1
Also called XX gonadal dysgenesis-deafness syndrome-without neurological manifestations
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:642945 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.