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Hereditary spherocytosis

Just diagnosed with Hereditary spherocytosis?

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

Open the full Hereditary spherocytosis hub →

Overview

Hereditary spherocytosis is a rare condition. Also known as Minkowski-Chauffard disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary spherocytosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:822 · OMIM 182900, 270970, 612653 · ICD-10 D58.0 · GARD 0006639

Find care for Hereditary spherocytosis

Authoritative references for Hereditary spherocytosis

Common questions

I was just diagnosed with Hereditary spherocytosis — what should I do first?

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

Where can I find a specialist for Hereditary spherocytosis?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hereditary spherocytosis, filtered to your area.

Are there clinical trials for Hereditary spherocytosis?

Tomeko shows live, recruiting studies for Hereditary spherocytosis 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