You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Chromosome 2q37 deletion syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Chromosome 2q37 deletion syndrome hub →Chromosome 2q37 deletion syndrome is a rare condition. Also known as Albright hereditary osteodystrophy type 3, Albright hereditary osteodystrophy-like syndrome, Brachydactyly-intellectual disability syndrome, Del(2)(q37), Deletion 2q37, Monosomy 2q37qter. Tomeko brings together the specialists, research, clinical trials, treatments and community for Chromosome 2q37 deletion syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1001 · OMIM 600430 · ICD-10 Q93.5 · GARD 0010202
Start by learning the basics from an authoritative source, find a specialist or center that sees Chromosome 2q37 deletion 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 Chromosome 2q37 deletion syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Chromosome 2q37 deletion syndrome from ClinicalTrials.gov on the hub.