You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Pontocerebellar hypoplasia, type 11, look for clinical trials, and connect with others living with it — all in one place.
Open the full Pontocerebellar hypoplasia, type 11 hub →Pontocerebellar hypoplasia, type 11 is a rare condition. Also known as PCH11, Pontocerebellar hypoplasia due to TBC1D23. Tomeko brings together the specialists, research, clinical trials, treatments and community for Pontocerebellar hypoplasia, type 11 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:611247 · OMIM 617695 · ICD-10 Q04.3 · GARD 0018029
Start by learning the basics from an authoritative source, find a specialist or center that sees Pontocerebellar hypoplasia, type 11, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Pontocerebellar hypoplasia, type 11, filtered to your area.
Tomeko shows live, recruiting studies for Pontocerebellar hypoplasia, type 11 from ClinicalTrials.gov on the hub.