CDH3 HJMD Resource
CDH3 · HJMD Contact

Gene: CDH3 (P-cadherin) Chromosome 16q22.1 Autosomal recessive

CDH3-related hypotrichosis with juvenile macular dystrophy (HJMD).

A resource for patients, caregivers and researchers.

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Patients

Plain-language information about HJMD, its effects on hair and central vision, and what is being studied.

Caregivers

Connect with other families, share experiences, and find specialists who know this condition.

Researchers

Reach families interested in natural-history studies, registries and future treatment research.

Contact us

Whether you've just received a diagnosis or you study cadherins, we'd like to hear from you. Send a message with the form, or email us directly.