You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Multiple congenital anomalies-hypotonia-seizures syndrome 3, look for clinical trials, and connect with others living with it — all in one place.
Open the full Multiple congenital anomalies-hypotonia-seizures syndrome 3 hub →Multiple congenital anomalies-hypotonia-seizures syndrome 3 is a rare condition. Also known as Congenital disorder of glycosylation due to PIGT deficiency, MCAHS type 3, Multiple congenital anomalies-hypotonia-seizures syndrome type 3, PIGT-CDG. Tomeko brings together the specialists, research, clinical trials, treatments and community for Multiple congenital anomalies-hypotonia-seizures syndrome 3 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:369837 · OMIM 615398 · ICD-10 E77.8 · GARD 0017584
Start by learning the basics from an authoritative source, find a specialist or center that sees Multiple congenital anomalies-hypotonia-seizures syndrome 3, 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 Multiple congenital anomalies-hypotonia-seizures syndrome 3, filtered to your area.
Tomeko shows live, recruiting studies for Multiple congenital anomalies-hypotonia-seizures syndrome 3 from ClinicalTrials.gov on the hub.