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Chromosome 3q29 microdeletion syndrome

Just diagnosed with Chromosome 3q29 microdeletion syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Chromosome 3q29 microdeletion syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full Chromosome 3q29 microdeletion syndrome hub →

Overview

Chromosome 3q29 microdeletion syndrome is a rare condition. Also known as 3q subtelomere deletion syndrome, 3qter deletion, Del(3)(q29), Monosomy 3q29, Monosomy 3qter. Tomeko brings together the specialists, research, clinical trials, treatments and community for Chromosome 3q29 microdeletion syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:65286 · OMIM 609425 · ICD-10 Q93.5 · GARD 0011974

Find care for Chromosome 3q29 microdeletion syndrome

Authoritative references for Chromosome 3q29 microdeletion syndrome

Common questions

I was just diagnosed with Chromosome 3q29 microdeletion syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Chromosome 3q29 microdeletion syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Chromosome 3q29 microdeletion syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Chromosome 3q29 microdeletion syndrome, filtered to your area.

Are there clinical trials for Chromosome 3q29 microdeletion syndrome?

Tomeko shows live, recruiting studies for Chromosome 3q29 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