Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Hydrolethalus syndrome 1

MONDO:0009365

Any hydrolethalus syndrome in which the cause of the disease is a mutation in the HYLS1 gene.

Also known as: hydrolethalus syndrome, HYLS1 hydrolethalus syndrome, hydrolethalus syndrome 1, hydrolethalus syndrome caused by mutation in HYLS1, hydrolethalus syndrome type 1, HLS1

1 clinical trial for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (679) Hereditary disease (176) Human disease (14) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0) Disease by etiologic mechanism (0) Hydrolethalus syndrome (0)
Trials to join now! 1
Sort by
  • Scientists map DNA 'Signatures' in rare fetal diseases

    Knowledge-focused Recruiting now

    This study looks at DNA methylation patterns (chemical tags on DNA) in fetuses with rare genetic diseases. Researchers will analyze DNA from amniotic fluid and tissue samples to create reference signatures. The goal is to improve diagnosis of these conditions before birth. The st…

    Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:01 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space