You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hao-Fountain syndrome due to 16p13.2 microdeletion, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hao-Fountain syndrome due to 16p13.2 microdeletion hub →Hao-Fountain syndrome due to 16p13.2 microdeletion is a rare condition. Also known as Chromosome 16p13.2 deletion syndrome, Del(16)(p13.2), Monosomy 16p13.2. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hao-Fountain syndrome due to 16p13.2 microdeletion so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:500055 · OMIM 616863 · ICD-10 Q93.5 · GARD 0017920
Start by learning the basics from an authoritative source, find a specialist or center that sees Hao-Fountain syndrome due to 16p13.2 microdeletion, 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 Hao-Fountain syndrome due to 16p13.2 microdeletion, filtered to your area.
Tomeko shows live, recruiting studies for Hao-Fountain syndrome due to 16p13.2 microdeletion from ClinicalTrials.gov on the hub.