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Ambras type hypertrichosis universalis congenita

Just diagnosed with Ambras type hypertrichosis universalis congenita?

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

Open the full Ambras type hypertrichosis universalis congenita hub →

Overview

Ambras type hypertrichosis universalis congenita is a rare condition. Also known as Ambras syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Ambras type hypertrichosis universalis congenita so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:1023 · OMIM 145701 · ICD-10 Q84.2 · GARD 0008206

Find care for Ambras type hypertrichosis universalis congenita

Authoritative references for Ambras type hypertrichosis universalis congenita

Common questions

I was just diagnosed with Ambras type hypertrichosis universalis congenita — what should I do first?

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

Where can I find a specialist for Ambras type hypertrichosis universalis congenita?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Ambras type hypertrichosis universalis congenita, filtered to your area.

Are there clinical trials for Ambras type hypertrichosis universalis congenita?

Tomeko shows live, recruiting studies for Ambras type hypertrichosis universalis congenita 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