You are not alone. Here is where to start: learn the basics, find a specialist or center that sees X-linked intellectual disability-retinitis pigmentosa syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full X-linked intellectual disability-retinitis pigmentosa syndrome hub →X-linked intellectual disability-retinitis pigmentosa syndrome is a rare condition. Also known as Aldred syndrome, Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion, Retinitis pigmentosa and intellectual disability due to del(X)(p11.3), Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3. Tomeko brings together the specialists, research, clinical trials, treatments and community for X-linked intellectual disability-retinitis pigmentosa syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:85332 · OMIM 300578 · ICD-10 H35.5 · GARD 0008360
Start by learning the basics from an authoritative source, find a specialist or center that sees X-linked intellectual disability-retinitis pigmentosa syndrome, 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 X-linked intellectual disability-retinitis pigmentosa syndrome, filtered to your area.
Tomeko shows live, recruiting studies for X-linked intellectual disability-retinitis pigmentosa syndrome from ClinicalTrials.gov on the hub.