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12p12.1 microdeletion syndrome

Just diagnosed with 12p12.1 microdeletion syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 12p12.1 microdeletion syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full 12p12.1 microdeletion syndrome hub →

Overview

12p12.1 microdeletion syndrome is a rare condition. Also known as Del(12)(p12.1), Monosomy 12p12.1. Tomeko brings together the specialists, research, clinical trials, treatments and community for 12p12.1 microdeletion syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:313884 · OMIM 616803 · ICD-10 Q93.5 · GARD 0017414

Find care for 12p12.1 microdeletion syndrome

Authoritative references for 12p12.1 microdeletion syndrome

Common questions

I was just diagnosed with 12p12.1 microdeletion syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees 12p12.1 microdeletion syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for 12p12.1 microdeletion syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat 12p12.1 microdeletion syndrome, filtered to your area.

Are there clinical trials for 12p12.1 microdeletion syndrome?

Tomeko shows live, recruiting studies for 12p12.1 microdeletion syndrome from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com