You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Alagille syndrome due to 20p12 microdeletion, look for clinical trials, and connect with others living with it — all in one place.
Open the full Alagille syndrome due to 20p12 microdeletion hub →Alagille syndrome due to 20p12 microdeletion is a rare condition. Also known as Alagille syndrome due to del(20)(p12), Alagille syndrome due to monosomy 20p12, Alagille-Watson syndrome due to monosomy 20p12, Arteriohepatic dysplasia due to monosomy 20p12, Syndromic bile duct paucity due to monosomy 20p12. Tomeko brings together the specialists, research, clinical trials, treatments and community for Alagille syndrome due to 20p12 microdeletion so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:261600 · OMIM 118450 · ICD-10 Q44.7 · GARD 0017250
Start by learning the basics from an authoritative source, find a specialist or center that sees Alagille syndrome due to 20p12 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 Alagille syndrome due to 20p12 microdeletion, filtered to your area.
Tomeko shows live, recruiting studies for Alagille syndrome due to 20p12 microdeletion from ClinicalTrials.gov on the hub.