You are not alone. Here is where to start: learn the basics, find a specialist or center that sees HNSHA due to aldolase A deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full HNSHA due to aldolase A deficiency hub →HNSHA due to aldolase A deficiency is a rare condition. Also known as GSD due to aldolase A deficiency, GSD type 12, GSD type XII, Glycogen storage disease type 12, Glycogen storage disease type XII, Glycogenosis due to aldolase A deficiency, Glycogenosis type 12, Glycogenosis type XII. Tomeko brings together the specialists, research, clinical trials, treatments and community for HNSHA due to aldolase A deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:57 · OMIM 611881 · ICD-10 E74.0 · GARD 0000600
Start by learning the basics from an authoritative source, find a specialist or center that sees HNSHA due to aldolase A deficiency, 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 HNSHA due to aldolase A deficiency, filtered to your area.
Tomeko shows live, recruiting studies for HNSHA due to aldolase A deficiency from ClinicalTrials.gov on the hub.